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MET mutation causes muscular dysplasia and arthrogryposis
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 pedigree charact...
Autores principales: | Zhou, Hang, Lian, Chengjie, Wang, Tingting, Yang, Xiaoming, Xu, Caixia, Su, Deying, Zheng, Shuhui, Huang, Xiangyu, Liao, Zhiheng, Zhou, Taifeng, Qiu, Xianjian, Chen, Yuyu, Gao, Bo, Li, Yongyong, Wang, Xudong, You, Guoling, Fu, Qihua, Gurnett, Christina, Huang, Dongsheng, Su, Peiqiang |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404111/ https://www.ncbi.nlm.nih.gov/pubmed/30777867 http://dx.doi.org/10.15252/emmm.201809709 |
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