Two closely spaced nonsense mutations in the DMD gene in a Malaysian family-Reference-Cited by-同舟云学术

Two closely spaced nonsense mutations in the DMD gene in a Malaysian family

Published:2011-07 Issue:3 Volume:103 Page:303-304
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Rani Abdul Qawee,Malueka Rusdy Ghazali,Sasongko Teguh Haryo,Awano Hiroyuki,Lee Tomoko,Yagi Mariko,Zilfalil Bin Alwi,Salmi A.B. Razak,Takeshima Yasuhiro,Zabidi-Hussin Z.A.M.H.,Matsuo Masafumi

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference17 articles.

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3. Dystrophin in frameshift deletion patients with Becker muscular dystrophy;Gangopadhyay;Am. J. Hum. Genet.,1992

4. Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy;Sifringer;Hum. Genet.,2004

5. Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysis;Saad;Am. J. Med. Genet.,1998

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1. Identification of two novel insertion abnormal transcripts in two Chinese families affected with Dystrophinopathy;Journal of Clinical Laboratory Analysis;2019-12-03

2. Mutation Spectrum ofDystrophinGene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy;Journal of Neurogenetics;2013-02-26

3. Transient hypermutability, chromothripsis and replication-based mechanisms in the generation of concurrent clustered mutations;Mutation Research/Reviews in Mutation Research;2012-01