Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study-Reference-Cited by-同舟云学术

Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study

Published:2013-06-12 Issue:1 Volume:22 Page:110-118
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Wei Xiaoming,Dai Yi,Yu Ping,Qu Ning,Lan Zhangzhang,Hong Xiafei,Sun Yan,Yang Guanghui,Xie Shuqi,Shi Quan,Zhou Hanlin,Zhu Qian,Chu Yuxing,Yao Fengxia,Wang Jinming,He Jingni,Yang Yun,Liang Yu,Yang Yi,Qi Ming,Yang Ling,Wang Wei,Wu Haitao,Duan Jing,Shen Cheng,Wang Jun,Cui Liying,Yi Xin

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201382.pdf

Reference26 articles.

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3. Aartsma-Rus A, Van Deutekom JC, Fokkema IF, Van Ommen GJ, Den Dunnen JT : Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve 2006; 34: 135–144.

4. Lalic T, Vossen RH, Coffa J et al: Deletion and duplication screening in the DMD gene using MLPA. Eur J Hum Genet 2005; 13: 1231–1234.

5. Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME : Microarray-based mutation detection in the dystrophin gene. Hum Mutat 2008; 29: 1091–1099.

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