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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986225/
https://www.ncbi.nlm.nih.gov/pubmed/27527345
http://dx.doi.org/10.1186/s12881-016-0322-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986225/
https://www.ncbi.nlm.nih.gov/pubmed/27527345
http://dx.doi.org/10.1186/s12881-016-0322-2

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