| Literature DB >> 22406499 |
Qian Xin1, Lin Li, Jiangxia Li, Rongfang Qiu, Chenhong Guo, Yaoqin Gong, Qiji Liu.
Abstract
Human synpolydactyly (SPD), belonging to syndactyly (SD) II, is an inherited autosomal-dominant limb malformation characterized by SD of finger 3 or 4 or toe 4 or 5, usually with digit duplication. Previous studies have demonstrated that homeobox protein D13 (HOXD13) is responsible for this Mendelian disorder. In this paper, we report on a family with SPD - 7 members show typical SPD malformations. We used PCR and Sanger sequencing of DNA from peripheral blood samples and found an 8-Ala expansion in exon 1 of HOXD13 by mutation detection; this variant was absent in unaffected members and in 50 unaffected non-related subjects. This study further confirmed the correlation between SPD and alanine expansion in HOXD13.Entities:
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Year: 2012 PMID: 22406499 DOI: 10.1016/j.gene.2012.02.046
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688