Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy-Reference-Cited by-同舟云学术

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Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy

Published:1993-01 Issue:1 Volume:3 Page:57-64
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Bushby K.M.D.,Goodship J.A.,Nicholson L.V.B.,Johnson M.A.,Haggerty I.D.,Gardner-Medwin D.

Publisher

Elsevier BV

Subject

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

Reference39 articles.

1. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy;Kunkel;Nature,1986

2. The manifesting carrier in Duchenne muscular dystrophy;Moser;Clin Genet,1974

3. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales;Norman;Clin Genet,1989

4. Myopathic changes in muscular dystrophy carriers;Dubowitz,1963

5. The detection of carriers of X-linked muscular dystrophy. A review of some methods studied in Newcastle upon Tyne;Gardner-Medwin;J Neurol Sci,1971

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