Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series

scientific article published on 01 March 2006

Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series is …
instance of (P31):
scholarly articleQ13442814

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P698PubMed publication ID16633967

P2093author name stringWeis J
Tolnay M
Burgunder JM
Ramelli GP
Joncourt F
Luetschg J
P433issue11-12
P921main subjectBecker muscular dystrophyQ2484592
P304page(s)189-193
P577publication date2006-03-01
P1433published inSwiss Medical WeeklyQ1321858
P1476titleBecker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series
P478volume136

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cites work (P2860)
Q36266919A case of Becker muscular dystrophy with early manifestation of cardiomyopathy
Q39032892A case report with the peculiar concomitance of 2 different genetic syndromes.
Q34459245A comprehensive database of Duchenne and Becker muscular dystrophy patients (0-18 years old) in East China
Q41010730A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene
Q37109015Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database
Q54269189Clinical Utility Gene Card for: Becker muscular dystrophy.
Q41854116Deletion mutations in Duchenne muscular dystrophy (DMD) in Western Saudi children
Q89435449Genotype-phenotype correlation in Becker muscular dystrophy in Chinese patients
Q37812049Pseudometabolic presentation of dystrophinopathy due to a missense mutation

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