Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)-Reference-Cited by-同舟云学术

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Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)

Published:1998-09 Issue:3 Volume:103 Page:323-327
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Kobayashi Kazuhiro,Nakahori Yutaka,Mizuno Kunihiko,Miyake Masashi,Kumagai Toshiyuki,Honma Akira,Nonaka Ikuya,Nakamura Yusuke,Tokunaga Katsushi,Toda T.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050824.pdf

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A 3000-year-old founder variant in the DRC1 gene causes primary ciliary dyskinesia in Japan and Korea;Journal of Human Genetics;2024-08-16

2. LAMA2gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes;Human Mutation;2018-08-10

3. Neonatal Neuromuscular Disorders;Avery's Diseases of the Newborn;2018

4. Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan;Journal of Human Genetics;2017-07-06

5. Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients;Brain and Development;2015-10

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