Identifying and circumventing the defect in Duchenne muscular dystrophy: Clinical and biochemical restoration after practical intervention-Reference-Cited by-同舟云学术

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Identifying and circumventing the defect in Duchenne muscular dystrophy: Clinical and biochemical restoration after practical intervention

Published:1987-10 Issue:2 Volume:24 Page:187-190
ISSN:0306-9877
Container-title:Medical Hypotheses
language:en
Short-container-title:Medical Hypotheses

Author:

Thomson W.H.S.

Publisher

Elsevier BV

Subject

General Medicine

Reference25 articles.

1. The neurogenic and myogenic hypotheses in human (Duchenne) muscular dystrophy;Thomson;Nature,1974

2. The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy;Thomson;Clin Chim Acta,1969

3. Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins;Gomez;Neurology,1977

4. The rate of spontaneous mutation of a human gene;Haldane;J Genet,1935

5. No sex difference in mutation rates of Duchenne muscular dystrophy;Yasuda;J Med Genet,1980

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Review Article: Dystrophin-Related Muscular Dystrophies;Journal of Child Neurology;1989-10

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