Heterogous Dystrophin mRNA Produced by a Novel Splice Acceptor Site Mutation in Intermediate Dystrophinopathy-Reference-Cited by-同舟云学术

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Heterogous Dystrophin mRNA Produced by a Novel Splice Acceptor Site Mutation in Intermediate Dystrophinopathy

Published:2003-01 Issue:1 Volume:53 Page:125-131
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Adachi Kayo,Takeshima Yasuhiro,Wada Hiroko,Yagi Mariko,Nakamura Hajime,Matsuo Masafumi

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference38 articles.

1. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy

2. Clinical investigation in duchenne dystrophy: 2. Determination of the ?power? of therapeutic trials based on the natural history

3. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

4. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

Cited by 12 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. Faulty RNA splicing: consequences and therapeutic opportunities in brain and muscle disorders;Human Genetics;2017-04-22

2. A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathy;Journal of Human Genetics;2014-05-29

3. Antisense suppression of donor splice site mutations in the dystrophin gene transcript;Molecular Genetics & Genomic Medicine;2013-06-13

4. Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center;Journal of Human Genetics;2010-05-20

5. Microarray-based mutation detection in thedystrophingene;Human Mutation;2008-09

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