Mutations in the δ-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)-Reference-Cited by-同舟云学术

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Mutations in the δ-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)

Published:1997-05-01 Issue:1 Volume:1 Page:49-58
ISSN:1364-6745
Container-title:neurogenetics
language:
Short-container-title:neurogenetics

Author:

Duggan David J.,Manchester David,Stears Karen P.,Mathews Dennis J.,Hart Carolyn,Hoffman Eric P.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s100480050008.pdf

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