Screening 25 Dystrophin Gene Exons for Deletions in Arab Children with Duchenne Muscular Dystrophy-Reference-Cited by-同舟云学术

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Screening 25 Dystrophin Gene Exons for Deletions in Arab Children with Duchenne Muscular Dystrophy

Published:1998 Issue:2 Volume:48 Page:61-66
ISSN:0001-5652
Container-title:Human Heredity
language:en
Short-container-title:Hum Hered

Author:

Haider M.Z.,Bastaki L.,Habib Y.,Moosa A.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 10 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. Inherited myopathies in the Middle East and North Africa;Gene Reports;2022-12

2. DMD ‐related muscular dystrophy in Cameroon: Clinical and genetic profiles;Molecular Genetics & Genomic Medicine;2020-06-15

3. Genetic and clinical profile of patients of Duchenne muscular dystrophy: Experience from a tertiary care center in Eastern India;Indian Pediatrics;2015-06

4. Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy;Egyptian Journal of Medical Human Genetics;2014-07

5. Intragenic deletion patterns of dystrophin gene in Duchenne and Becker muscular dystrophy patients from Algeria;Genes & Genomics;2013-08-14

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