Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?

scientific article published on 01 January 1993

Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype? is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1093/HMG/2.1.39
P698PubMed publication ID8490621

P50authorMayana ZatzQ2920198
Mariz VainzofQ48427302
Maria Rita Passos-BuenoQ78114430
P2093author name stringR C Pavanello
R I Takata
P433issue1
P921main subjectphenotypeQ104053
Becker muscular dystrophyQ2484592
P304page(s)39-42
P577publication date1993-01-01
P1433published inHuman Molecular GeneticsQ2720965
P1476titleIs the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
P478volume2

Reverse relations

cites work (P2860)
Q70485043A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient
Q35888853A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy
Q36420910Assessing pathogenicity for novel mutation/sequence variants: the value of healthy older individuals
Q33596173Deletions in the 5' region of dystrophin and resulting phenotypes
Q49428049Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype
Q39036803Dystrophin genotype-cardiac phenotype correlations in Duchenne and Becker muscular dystrophies using cardiac magnetic resonance imaging
Q72640306Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice
Q34119276Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin
Q40539157Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin
Q34445717Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation
Q37217303Neuromuscular disorders: genes, genetic counseling and therapeutic trials
Q36101284Spectrin, alpha-actinin, and dystrophin
Q57039821Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy
Q30376293The Dystrophin Complex: Structure, Function, and Implications for Therapy

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