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Qaagi - Book of Why

Causes

Effects

point mutationscausingmethylmalonic aciduria

maternal vitamin B12 deficiency in three infants with severe illness Cvitanovic Sojat , L. ; Jurcic , Z. ; Fumic , K. ; Juricic , L. ; Erwa , W. ; D.M.irleir , L. ; Gerlot , E. ; Mucic , B. ; Vezmar , V. , 1996(passive) caused byMethylmalonic aciduria

a deficiency of meth - ylmalonyl - CoA carboxylase activity that is a result of a defect either in the apoenzyme or in the active form of vitamin B12(passive) is caused byMethylmalonic aciduria

a deficiency of methylmalonyl - CoA carboxylase activity that is a resouflt a defect either in the apoenzyme or in bestbinaryoptionstrading com active form of vitaminI312(passive) is caused byMethylmalonic aciduria

reduced activity of vitamin B12 dependent methylmalonyl - CoA mutase(passive) caused bymethylmalonic aciduria

a deficiency of methylmalonyl - CoA carboxylase activity that is a resouflt a defect either in the apoenzyme or in binary option probability calculator active form of vitaminI312(passive) is caused byMethylmalonic aciduria

a deficiency of methylmalonyl - CoA binary option forex trading strategy activity that is a resouflt a defect either in the apoenzyme or in the active form of vitaminI312(passive) is caused byMethylmalonic aciduria

Defective AMN causes hereditary megaloblastic anemia 1 ; Defective BTD causes biotidinase deficiencycausesmethylmalonic aciduria

defects in MUT(passive) caused bymethylmalonic aciduria

D. Cardiovascularhypercalcemiamay causemethylmalonic aciduria

The Senses 415 end - organ receptors , and anti - inflammatory medicationsmay causemethylmalonic aciduria

NomenclatureThe nomenclature for inherited disorders of intracellular cobalamin transport and processing is based on cellular complementation analysis that defines cobalamin groups A - G ( cblA - cblG).In general , cobalamin disorders are classified into those that affect MUT only (causingmethylmalonic aciduria

a homologous mutation at cytogenetic location , 12q24.11(passive) is caused byMethylmalonic aciduria

that pulmonary thromboembolismmay causemethylmalonic aciduria

Hg decrease in blood pressure andmay causemethylmalonic aciduria

the mechanical causes venous obstructionmay causemethylmalonic aciduria

Stress fracturesmay causemethylmalonic aciduria

mutation in MUT gene [ 45(passive) is caused byMethylmalonic aciduria

Defective CD320causesmethylmalonic aciduria

It is also usedto preventmethylmalonic aciduria

from deficiency of enzyme argininosuccinate lyase ( ASLresultsfrom deficiency of enzyme argininosuccinate lyase ( ASL

lethargy , poor appetite , developmental delay , intellectual disability , and a poorly controlled breathing rate or body temperaturecauseslethargy , poor appetite , developmental delay , intellectual disability , and a poorly controlled breathing rate or body temperature

to a person remaining with undiagnosed Argininosuccinic acidurialeadingto a person remaining with undiagnosed Argininosuccinic aciduria

neurological problems as well as eventual damage to the livercausesneurological problems as well as eventual damage to the liver

to mental retardation and developmental abnormalities.[1leadingto mental retardation and developmental abnormalities.[1

loss(passive) caused byloss

in globus pallidus necrosisresultingin globus pallidus necrosis

in neonatal lethalityresultingin neonatal lethality

in 1967).Wewas ... discoveredin 1967).We

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