Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.

Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.

<h4>Background</h4>Syndactyly type 1 (SD1) is an autosomal dominant limb malformation characterized in its classical form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. Its four subtypes (a, b, c, and d) are defined based on variable...

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Bibliographic Details
Main Authors: Limeng Dai, Dan Liu, Min Song, Xueqing Xu, Gang Xiong, Kang Yang, Kun Zhang, Hui Meng, Hong Guo, Yun Bai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0096192&type=printable
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