MET mutation causes muscular dysplasia and arthrogryposis

MET mutation causes muscular dysplasia and arthrogryposis

Abstract Arthrogryposis is a group of phenotypically and genetically heterogeneous disorders characterized by congenital contractures of two or more parts of the body; the pathogenesis and the causative genes of arthrogryposis remain undetermined. We examined a four‐generation arthrogryposis pedigre...

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Bibliographic Details
Main Authors: Hang Zhou, Chengjie Lian, Tingting Wang, Xiaoming Yang, Caixia Xu, Deying Su, Shuhui Zheng, Xiangyu Huang, Zhiheng Liao, Taifeng Zhou, Xianjian Qiu, Yuyu Chen, Bo Gao, Yongyong Li, Xudong Wang, Guoling You, Qihua Fu, Christina Gurnett, Dongsheng Huang, Peiqiang Su
Format: Article
Language:English
Published: Wiley 2019-03-01
Series:EMBO Molecular Medicine
Subjects:
arthrogryposis
MET
muscle development
muscular dysplasia
whole‐exome sequence
Online Access:https://doi.org/10.15252/emmm.201809709

Internet

https://doi.org/10.15252/emmm.201809709

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