Congenital muscular dystrophy with primary laminin ?2 (merosin) deficiency presenting as inflammatory myopathy-Reference-Cited by-同舟云学术

Congenital muscular dystrophy with primary laminin ?2 (merosin) deficiency presenting as inflammatory myopathy

Published:1996-11 Issue:5 Volume:40 Page:782-791
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Pegoraro Elena,Cianno Brad Di,Hoffman Eric P.,Mancias Pedro,Swerdlow Steven H.,Raikow Radmila B.,Garcia Carlos,Marks Harold,Crawford Thomas,Carver Virginia

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference44 articles.

1. A colour atlas of muscle disorders in childhood. London: Wolfe Medical, 1989

2. The congenital muscular dystorphies. In: eds. Myology, vol 1. New York: McGraw-Hill Book, 1994:1275-1289

3. Congenital progressive muscular dystrophy of the fukuyama type — clinical, genetic and pathological considerations —

4. Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33

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