Allele frequencies of intragenic, and 5′ and 3′ markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy-Reference-Cited by-同舟云学术

Allele frequencies of intragenic, and 5′ and 3′ markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy

Published:1996-12 Issue:4 Volume:41 Page:391-397
ISSN:0021-5074
Container-title:Japanese Journal of Human Genetics
language:en
Short-container-title:Jap J Human Genet

Author:

Tsukamoto Hiroko,Inui Koji,Fukushima Hisao,Okada Shintaro

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/jhg199636.pdf

Reference26 articles.

1. Akita Y, Ohno S, Goto J, Nakano I, Takatsu M, Sugita H, Suzuki K (1987): Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism. Jpn J Hum Genet32: 71–82

2. Al-Maghtheh M, Ray V, Mastana SS, Garralda MD, Bhattacharya SS, Papiha SS (1993): Variation in DNA polymorphisms of the short arm of the human X chromosome: genetic affinity of Parsi from Western India. Hum Hered43: 239–243

3. Beggs AH, Koenig M, Boyce FM, Kunkel LM (1990): Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet86: 45–48

4. Beggs AH, Kunkel LM (1990): A polymorphic CACA repeat in the 3′ untranslated region of dystrophin. Nucleic Acids Res18: 1931

5. Camberlain JS, Gibbs RA, Ranier JE, Nguyen PN, Caskey CT (1988): Deletion screening of the Duchenne muscular dystrophy locusvia multiplex DNA amplification. Nucleic Acids Res16: 11141–11156

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2. Identificación de deleciones en el gen de la distrofina y detección de portadoras en familias con distrofia muscular de Duchenne/Becker;Revista de Neurología;2009

3. Prenatal Diagnosis of Duchenne Muscular Dystrophy in the Japanese Population by Fluorescent CA Repeat Polymorphisms Analysis;Journal of Obstetrics and Gynaecology Research;1997-10