Restoration of half the normal dystrophin sequence in a double-deletion Duchenne muscular dystrophy family-Reference-Cited by-同舟云学术

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Restoration of half the normal dystrophin sequence in a double-deletion Duchenne muscular dystrophy family

Published:1994-02-01 Issue:3 Volume:49 Page:323-327
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hoop R. C.,Russo L. S.,Riconda D. L.,Schwartz L. S.,Hoffman E. P.

Publisher

Wiley

Subject

Genetics (clinical)

Reference20 articles.

1. INHERITED DELETION AT DUCHENNE DYSTROPHY LOCUS IN NORMAL MALE

2. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

3. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

4. (1988): Multiplex PCR for the diagnosis of Duchenne muscular dystrophy. In (eds): “PCR Protocols: A Guide to Methods and Applications.” Orlando: Academic Press. pp 272-281.

Cited by 13 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. Prenatal risk assessment of Xp21.1 duplication involving theDMDgene by optical genome mapping;Life Science Alliance;2024-08-08

2. Two mutations in one dystrophin gene;Neurologia i Neurochirurgia Polska;2013

3. Dystrophinopathies;Handbook of Clinical Neurology;2011

4. Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations;Behavioral and Brain Functions;2008-04-29

5. Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule;Human Mutation;2008-03-17

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