mutations in the dystrophin gene , which encodes the protein dystrophin(passive) is caused byBecker 's muscular dystrophy
mutations in the dystrophin gene on the short arm of the X - chromosome ( Xp21(passive) caused byBecker muscular dystrophy ( BMD
mutations in the dystrophin gene with variable phenotypes(passive) is caused byBecker muscular dystrophy ( BMD
mutations of the dystrophin gene on the X chromosome(passive) caused byBecker muscular dystrophy
mutations in the dystrophin gene that leads to misshapen dystrophinleadsto Becker muscular dystrophy
an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene(passive) caused by03/01/2009 - " Becker muscular dystrophy
abnormalities ( mutations ) in the dmd gene that is responsible for the production of the dystrophin protein dystrophin(passive) is caused byBecker muscular dystrophy
a different type of mutation in the dystrophin gene(passive) is caused byBecker muscular dystrophy
mutations in the dystrophin gene ... and the pattern of inheritance is X - linked recessive(passive) is caused byBecker muscular dystrophy
mutations of the DMD gene located at Xp21.[4(passive) are caused byBecker muscular dystrophy ( BMD
deletions / duplications and point mutations in the DMD genecauseDuchenne and Becker muscular dystrophy
less significant mutations in the same dystrophin gene with higher levels of functioning dystrophin found in myocytes(passive) is caused byBecker ’s muscular dystrophy
the same gene mutation(passive) caused byBecker muscular dystrophy
a change , or mutation , in the DMD gene(passive) is caused byDuchenne / Becker Muscular Dystrophy
in - frame deletions of the dystrophin gene(passive) is ... caused byBecker muscular dystrophy
mutations of the X chromosome dystrophin ( DMD ) gene that lead to partial deficiency of dystrophin protein in patient skeletal muscle and heart ( Hoffman et al . 1989(passive) is caused byBecker muscular dystrophy ( BMD
an error in the dystrophin gene(passive) is caused byBecker muscular dystrophy
defects in the dystrophin gene(passive) are caused byDuchenne and Becker muscular dystrophy
the human DMD gene , mutations in whichcauseDuchenne and Becker muscular dystrophy
in - frame dystrophin gene mutations(passive) is ... caused byBecker muscular dystrophy ( BMD
exon 2-truncating mutation of DMD on November 17 , 2019 at 7:28 pm Nonsense and frameshift mutations of the dystrophin ( DMD ) gene(passive) caused byBecker muscular dystrophy
630 genesetsBecker muscular dystrophy
X - chromosomal DMD genecausingDuchenne and Becker muscular dystrophy
specific mutations in the gene for the dystrophin protein(passive) caused byBecker muscular dystrophy ( BMD
mutations of the X - linked dystrophin gene(passive) are caused byBecker muscular dystrophy ( BMD
his talk on the nature of the dystrophin gene and mutationscauseDuchenne and Becker muscular dystrophy
in - frame dystrophin gene deletionscausingBecker muscular dystrophy ( BMD
a mutation in the dmd dystrophin gene(passive) caused bybecker muscular dystrophy
dystrophin gene non - deletion / duplication mutationscausingBecker muscular dystrophy
a truncated , but partially functional DMD gene(passive) caused byBecker muscular dystrophy
mutations in the same gene encoding dystrophin(passive) are caused byDuchenne and Becker muscular dystrophy
partial absence of dystrophin(passive) is caused byBecker Muscular Dystrophy ( BMD
a single exon 48 deletion of the dystrophin gene(passive) caused byBecker muscular dystrophy
in - frame mutationsleadto milder Becker muscular dystrophy
changes the same gene , dystrophin , as in DMD(passive) is caused byBecker muscular dystrophy
A broad mutational spectrum in the dystrophin ( DMD ) gene , from large deletions / duplications to point mutationscausesDuchenne / Becker muscular dystrophy
Duchenne muscular dystrophy ... the gene defectcausesBecker muscular dystrophy
a certain type of genetic mutation(passive) caused byBecker muscular dystrophy ( BMD
that exon 25 is spliced out in the +1G→A mutation in intron 25 ,resultingin mild Becker muscular dystrophy
a reduction , rather than complete absence of dystrophin expression(passive) is caused byBecker muscular dystrophy
the muscle damage(passive) caused bythe muscle damage
to slowly worsening disabilityleadsto slowly worsening disability
from the skipping of four contiguous exons(71 - 74 ) of the dystrophin gene during mRNA maturation " Procresultingfrom the skipping of four contiguous exons(71 - 74 ) of the dystrophin gene during mRNA maturation " Proc
from dystrophin mutationsalso resultsfrom dystrophin mutations
from mutations in the same generesultsfrom mutations in the same gene
from nonsense mutationsresultingfrom nonsense mutations
long - term disability ... muscles that are used to breathecauseslong - term disability ... muscles that are used to breathe
from mutations in dystrophin ... and in the dystroglycanopathiesresultsfrom mutations in dystrophin ... and in the dystroglycanopathies
107 - 113 , 2008 Authors : Sura , Thanyachai | Eu - ahsunthornwattana , Jakris | Pingsuthiwong , Sarinee | Busabaratana , Manisa Abstract : Background : Duchenne muscular dystrophy ( DMD ) , a lethal X - linked disease affecting 1 in 3500 male births , and its more benign variant(passive) are caused107 - 113 , 2008 Authors : Sura , Thanyachai | Eu - ahsunthornwattana , Jakris | Pingsuthiwong , Sarinee | Busabaratana , Manisa Abstract : Background : Duchenne muscular dystrophy ( DMD ) , a lethal X - linked disease affecting 1 in 3500 male births , and its more benign variant
from mutations within the gene encoding dystrophinresultfrom mutations within the gene encoding dystrophin
muscle weakness and atrophycausesmuscle weakness and atrophy
alsocausedalso
a milder but still debilitating form of muscular dystrophyresultsa milder but still debilitating form of muscular dystrophy
in decreased dystrophinresultsin decreased dystrophin
from a mutated DMD generesultsfrom a mutated DMD gene
progressive muscle weakness from the hips down the legscausesprogressive muscle weakness from the hips down the legs
from expression of a partially functional protein product or insufficient dystrophin contentresultsfrom expression of a partially functional protein product or insufficient dystrophin content
generallyleadsgenerally
The muscle deterioration(passive) caused byThe muscle deterioration
Duchenne ( DMD ) and(passive) are causedDuchenne ( DMD ) and
weakness and muscle wastingcausesweakness and muscle wasting
to mutation of the dystrophin gene which reduced the synthesis of the dystrophinmay leadto mutation of the dystrophin gene which reduced the synthesis of the dystrophin
muscle weakness throughout my bodycausesmuscle weakness throughout my body
progressive deterioration and weakness in certain muscle groupscausesprogressive deterioration and weakness in certain muscle groups
from in - frame deletions in the DMD gene that allow synthesis of an internally truncated , but functional proteintypically resultsfrom in - frame deletions in the DMD gene that allow synthesis of an internally truncated , but functional protein
to dystrophin protein productioncontributingto dystrophin protein production
adaxialcausesadaxial
by in - frame dystrophin deletions that allow the production of an internally deleted but partially functional dystrophincausedby in - frame dystrophin deletions that allow the production of an internally deleted but partially functional dystrophin
less severe symptoms than Duchenne MDcausesless severe symptoms than Duchenne MD