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-Reference-Cited by-同舟云学术

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

Published:1992-02-15 Issue:4 Volume:42 Page:453-457
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kitoh Yoshihiko,Matsuo Masafumi,Nishio Hisahide,Takumi Toru,Nakajima Toshihiro,Masumura Takehiro,Koga Junichi,Nakamura Hajime

Publisher

Wiley

Subject

Genetics (clinical)

Reference18 articles.

1. Improved diagnosis of Duchenne/Becker muscular dystrophy.

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

3. High resoluation deletion breakpoint mapping in the DMD gene by whole cosmid hybridization

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

5. (1990) Multiplex PCR for the diagnosis of Duchenne muscular dystrophy. In (eds), “PCR Protocols”. San Diego, Academic Press, pp 272-281.

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

2. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal;Journal of the Neurological Sciences;2007-01

3. A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy;Chinese Medical Journal;2006-07

4. Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis;Brain and Development;1998-04

5. Screening 25 Dystrophin Gene Exons for Deletions in Arab Children with Duchenne Muscular Dystrophy;Human Heredity;1998