Mutation Spectrum ofDystrophinGene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy-Reference-Cited by-同舟云学术

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Mutation Spectrum ofDystrophinGene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy

Published:2013-02-26 Issue:1-2 Volume:27 Page:11-15
ISSN:0167-7063
Container-title:Journal of Neurogenetics
language:en
Short-container-title:Journal of Neurogenetics

Author:

Rani Abdul Qawee,Sasongko Teguh Haryo,Sulong Sarina,Bunyan David,Salmi Abdul Razak,Zilfalil Bin Alwi,Matsuo Masafumi,Zabidi-Hussin Z. A. M. H.

Publisher

Informa UK Limited

Subject

Cellular and Molecular Neuroscience,Genetics

Link

http://www.tandfonline.com/doi/pdf/10.3109/01677063.2012.762580

Reference16 articles.

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

2. ESEfinder: a web resource to identify exonic splicing enhancers

3. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

4. More deletions in the 5′ region than in the central region of the dystrophin gene were identified among filipino duchenne and becker muscular dystrophy patients

5. Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family

Cited by 8 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. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients;F1000Research;2023-11-17

2. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients;F1000Research;2023-02-07

3. Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy;Genes;2023-01-14

4. Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49–51 deletion phenotype;Molecular Genetics & Genomic Medicine;2022-11-24

5. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients;F1000Research;2022-02-07

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