Identification of a Novel Missense FBN2 Mutation in a...

PLoS ONE 2016 / 5 Vol. 11; Iss. 5

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing

Deng, Hao, Lu, Qian, Xu, Hongbo, Deng, Xiong, Yuan, Lamei, Yang, Zhijian, Guo, Yi, Lin, Qiongfen, Xiao, Jingjing, Guan, Liping, Song, Zhi, Wu, Zhi-Ying
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Volume:
11
Language:
english
Journal:
PLOS ONE
DOI:
10.1371/journal.pone.0155908
Date:
May, 2016
File:
PDF, 1.20 MB
english, 2016
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