Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers-Reference-Cited by-同舟云学术

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Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers

Published:1991-01 Issue:6 Volume:1 Page:397-409
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Marini Jean-François,Pons Françoise,Leger Jocelyne,Loffreda Nathalie,Anoal Monique,Chevallay Martine,Fardeau Michel,Leger Jean J.

Publisher

Elsevier BV

Subject

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

Reference37 articles.

1. Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy;Arahata;N Engl J Med,1989

2. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle;Ervasti;Nature,1990

3. Muscle Biopsy: A Modern Approach;Dubowitz,1973

4. Patterns of abnormal histochemical fiber type differentiation in human muscle biopsies;Johnson;J Neurol Sci,1978

5. The significance of type 2C muscle fibers in Duchenne muscular dystrophy;Nonaka;Muscle Nerve,1981

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