Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion-Reference-Cited by-同舟云学术

Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion

Published:2008-11-14 Issue:2 Volume:39 Page:239-243
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Ferreiro Verónica,Giliberto Florencia,Muñiz García M. Noelia,Francipane Liliana,Marzese Diego M.,Mampel Alejandra,Roqué María,Frechtel Gustavo D.,Szijan Irene

Funder

CONICET

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.21193/fullpdf

Reference13 articles.

1. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy;Béroud;Hum Mutat,2007

2. Function and genetics of dystrophin and dystrophin-related proteins in muscle;Blake;Physiol Rev,2002

3. Asymptomatic or minimally symptomatic hyperCKemia: histopathologic correlates;Dabby;Isr Med Assoc J,2006

4. Detection of germline mosaicism in two Duchenne muscular dystrophy families using polimorphic dinucleotide (CA)n repeat loci within the dystrophin gene;Ferreiro;Mol Diagn,2004

5. The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis;Ferreiro;Mol Diagn,2005

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