Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients-Reference-Cited by-同舟云学术

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Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients

Published:2013-11-14 Issue:1 Volume:59 Page:46-50
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Lee Tomoko,Takeshima Yasuhiro,Kusunoki Noriko,Awano Hiroyuki,Yagi Mariko,Matsuo Masafumi,Iijima Kazumoto

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg2013119.pdf

Reference17 articles.

1. Emery, A. E. The muscular dystrophies. Lancet. 23, 687–695 (2002).

2. Ahn, A. H. & Kunkel, L. M. The structural and functional diversity of dystrophin. Nat. Genet. 3, 283–291 (1993).

3. Takeshima, Y., Yagi, M., Okizuka, Y., Awano, H., Zhang, Z., Yamauchi, Y. et al. Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center. J. Hum. Genet. 55, 379–388 (2010).

4. Monaco, A. P., Bertelson, C. J., Liechti-Gallati, S., Moser, H. & Kunhekel, L. M. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 2, 90–95 (1988).

5. Haldane, J. B. The rate of spontaneous mutation of a human gene. J. Genet 31, 317–326 (1935).

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