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-Reference-Cited by-同舟云学术

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

Published:1995-11-06 Issue:2 Volume:59 Page:266-267
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Cutiongco Eva Malia,Padilla Carmencita D.,Takenaka Kaori,Yamasaki Yuko,Matsuo Masafumi,Nishio Hisahide

Publisher

Wiley

Subject

Genetics(clinical)

Reference13 articles.

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

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

3. 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

4. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

5. Amplification of ten deletion-rich exons of the dystrophin gene by polymerase chain reaction shows deletions in 36 of 90 Japanese families with Duchenne muscular dystrophy

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

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

3. Deletion mutations in Duchenne muscular dystrophy (DMD) in Western Saudi children;Saudi Journal of Biological Sciences;2010-07

4. Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients;Pediatrics International;2008-04

5. Comparative study on deletions of the dystrophin gene in three Asian populations;Journal of Human Genetics;2002-10