Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese population

BACKGROUND: Nonsyndromic orofacial cleft is a common birth defect with a complex etiology, including multiple genetic and environmental risk factors. Recent whole genome analyses suggested associations between nonsyndromic orofacial cleft and up to 18 genetic risk loci (ABCA4, BMP4, CRISPLD2, GSTT1,...

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Bibliografski detalji
Izdano u:BMC Med Genet
Glavni autori: Peng, Hsiu-Huei, Chang, Nai-Chung, Chen, Kuo-Ting, Lu, Jang-Jih, Chang, Pi-Yueh, Chang, Shih-Cheng, Wu-Chou, Yah-Huei, Chou, Yi-Ting, Phang, Wanni, Cheng, Po-Jen
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4986225/
https://ncbi.nlm.nih.gov/pubmed/27527345
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0322-2
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