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Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly
Camptodactyly is a digit deformity characterized by permanent flexion contracture of one or both fifth fingers at the proximal interphalangeal joints. Though over 60 distinct types of syndromic camptodactyly have been described, only one disease locus (3q11.2-q13.12) for nonsyndromic camptodactyly h...
Autores principales: | Deng, Hao, Deng, Sheng, Xu, Hongbo, Deng, Han-Xiang, Chen, Yulan, Yuan, Lamei, Deng, Xiong, Yang, Shengbo, Guan, Liping, Zhang, Jianguo, Yuan, Hong, Guo, Yi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880340/ https://www.ncbi.nlm.nih.gov/pubmed/27223613 http://dx.doi.org/10.1371/journal.pone.0155180 |
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