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Smart Reasoning:

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Qaagi - Book of Why

Causes

Effects

the cell reactionscausemuscle degeneration for people with muscular dystrophy

by in - frame mutations in the dystrophin gene(passive) caused bymuscular dystrophy ( DMD

a diseasecausesmuscle wasting , like muscular dystrophy

by mutations in CAPN3 gene(passive) caused bymuscular dystrophy ( LGMD2A

toxic proteinscausingmuscular dystrophy People

Lack of this vitaminalso causesa muscle ailment ( Muscular dystrophy

the genescausedifferent types of muscular dystrophy muscle

a disease - causing mutation , such as thosecausemuscle wasting in Duchenne muscular dystrophy

the known pathogenic variants likelyto causeMuscular Dystrophy and Muscular Myopathy

mutations in DMD gene which codes for protein dystrophin(passive) is caused byDuchenne muscular dystrophy

a defective gene for dystrophin ( a protein in the muscles).(passive) is caused byDuchenne muscular dystrophy

a defective gene for dystrophin ( a protein in the muscles(passive) is caused byDuchenne muscular dystrophy

mutations in the stop codon in the dystrophin gene , the largest known human gene which is responsible for the production of the protein dystrophin(passive) is caused byDuchenne Muscular Dystrophy

a [ [ mutation ] ] in the [ [ dystrophin ] ] gene which is located on the human [ [ X chromosome(passive) is caused byDuchenne [ [ muscular dystrophy

by a mutation in the dystrophin gene which is located on the human X chromosome(passive) is caused byDuchenne muscular dystrophy

mutations in the dystrophin gene , which results in muscle degeneration(passive) is caused byDuchenne muscular dystrophy

a mutation in the dystrophin gene , which results in the absence of full - length dystrophin protein , needed to protect muscles(passive) is caused byDuchenne muscular dystrophy

mutations in the dystrophin gene that contains the information for making dystrophin protein(passive) is caused byDuchenne muscular dystrophy

mutations in the DMD gene , which is located on the X chromosome(passive) is caused byDuchenne muscular dystrophy

different mutations in the dystrophin gene which is located on the human X chromosome including:[1][2(passive) is caused byDuchenne muscular dystrophy

a mutation of the dystrophin gene which is present on the X chromosome(passive) is caused byDuchenne Muscular Dystrophy

a mutation of the dystrophin gene at(passive) is caused byDuchenne muscular dystrophy

a mutation in the dystrophin gene(passive) is caused byDuchenne muscular dystrophy

an absence of dystrophin , a protein that helps keep muscle cells intact(passive) is caused byDuchenne Muscular Dystrophy

by the lack of a muscle - specific protein , dystrophin(passive) is causedDuchenne muscular dystrophy

frame - shift or nonsense mutation in the DMD gene(passive) is caused byDuchenne muscular dystrophy

due to the absence of dystrophin , a protein that helps keep muscle cells intact(passive) is causedDuchenne muscular dystrophy

A mutation of the dystrophin gene that eliminates dystrophin productioncausesDUCHENNE MUSCULAR DYSTROPHY

mutations of the DMD gene(passive) is caused byDuchenne muscular dystrophy

the absence of functional dystrophin protein(passive) is caused byDuchenne muscular dystrophy

dystrophin gene mutations which lead to the absence of the protein dystrophin(passive) is caused by Duchenne muscular dystrophy

DNA spelling errors in a gene responsible for producing a protein called dystrophin(passive) is caused byDuchenne muscular dystrophy

by the absence of the protein , dystrophin(passive) is causedDuchenne muscular dystrophy

the absence of the protein , dystrophin(passive) is caused byDuchenne muscular dystrophy

mutations of whichmay causeforms of muscular dystrophy

loss of function mutations of the X - linked DMD gene(passive) is caused byDuchenne muscular dystrophy

a mutation ... dystrophin productioncausesDuchenne muscular dystrophy

by a lack of the protein dystrophin in muscle fibres(passive) is causedDuchenne muscular dystrophy

the faulty signallingleadsto muscle damage in muscular dystrophy

a mutation of the dystrophin gene at locus Xp21.Approximately(passive) is caused byDuchenne muscular dystrophy

muscles to weaken and breakdown over timecausemuscles to weaken and breakdown over time

the skeletal muscles to become weakercausethe skeletal muscles to become weaker

to increasing weakening plus breakdown of your skeletal muscles over timeleadto increasing weakening plus breakdown of your skeletal muscles over time

geenticallyare causedgeentically

weaknesscausingweakness

of weakening or breakdown of skeletal musclescausesof weakening or breakdown of skeletal muscles

weakening of musclescausingweakening of muscles

to muscular weakeningleadto muscular weakening

in increasing weakening and breakdown of skeletal muscles over timeresultsin increasing weakening and breakdown of skeletal muscles over time

in increasing weakening and degeneration of skeletal musclesresultsin increasing weakening and degeneration of skeletal muscles

in increasing weakening and break down of skeletal muscles over timeresultsin increasing weakening and break down of skeletal muscles over time

to reduce mobility because of neurological weakness in the musclesleadto reduce mobility because of neurological weakness in the muscles

in increasing weakening and breakdown of skeletal musclesresultsin increasing weakening and breakdown of skeletal muscles

to reduced mobility because of neurological weakness in the musclesleadto reduced mobility because of neurological weakness in the muscles

the skeletal muscles to become weakercausethe skeletal muscles to become weaker

in increasing weakening and breakdown of skeletal muscles over timeresultsin increasing weakening and breakdown of skeletal muscles over time

the weakening and breakdown of skeletal muscles over a period of timecausesthe weakening and breakdown of skeletal muscles over a period of time

your symptoms such as Multiple Sclerosismay be causingyour symptoms such as Multiple Sclerosis

to premature deathcould ... leadto premature death

to early deathleadsto early death

walking difficulties along with other problemsmay causewalking difficulties along with other problems

muscle degeneration and weaknesscausesmuscle degeneration and weakness

to degeneration of skeletal and heart musclesleadsto degeneration of skeletal and heart muscles

progressive weakness in the skeletal musclescausesprogressive weakness in the skeletal muscles

to progressive deterioration in skeletal and cardiac muscle functionleadsto progressive deterioration in skeletal and cardiac muscle function

to a progressive muscle - wasting diseaseleadsto a progressive muscle - wasting disease

from a nonsense mutation in the dystrophin generesultingfrom a nonsense mutation in the dystrophin gene

muscles to weaken and waste over timecausesmuscles to weaken and waste over time

muscle weakness and deteriorationcausesmuscle weakness and deterioration

to progressively worsening disabilityleadsto progressively worsening disability

in respiratory muscle and heart muscle failurelater resultsin respiratory muscle and heart muscle failure

muscle damage(passive) caused bymuscle damage

progressive weakness and muscle degenerationcausesprogressive weakness and muscle degeneration

The X - linked muscle - wasting disease(passive) is causedThe X - linked muscle - wasting disease

heart damage(passive) caused byheart damage

ptosis , dysphagia , and limb weaknesscausesptosis , dysphagia , and limb weakness

a progressive weakening and loss of muscle function over timecausesa progressive weakening and loss of muscle function over time

progressive weakness and loss of muscle masscausesprogressive weakness and loss of muscle mass

progressive weakness and loss of muscle masscauseprogressive weakness and loss of muscle mass

rapidly - worsening muscle weakness that starts in the legs and pelviscausesrapidly - worsening muscle weakness that starts in the legs and pelvis

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Smart Reasoning:

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