Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation-Reference-Cited by-同舟云学术

Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation

Published:2003-12 Issue:10 Volume:13 Page:779-787
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Kefi M,Amouri R,Driss A,Ben Hamida C,Ben Hamida M,Kunkel L.M,Hentati F

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference28 articles.

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3. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12;Lim;Nat Genet,1995

4. Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy;Noguchi;Science,1995

5. Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein;Nigro;Hum Mol Gen,1996

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