TFAP2B mutation and dental anomalies

Mutations inTFAP2B has been reported in patients with isolated patent ductus arteriosus (PDA) and Char syndrome. We performed mutation analysis of TFAP2B in 43 patients with isolated PDA, 7 patients with PDA with other congenital heart defects and 286 patients with isolated tooth agenesis with or wi...

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Detalles Bibliográficos
Autores principales: Tanasubsinn, Natchaya, Sittiwangkul, Rekwan, Pongprot, Yupada, Kawasaki, Katsushige, Ohazama, Atsushi, Sastraruji, Thanapat, Kaewgahya, Massupa, Kantaputra, Piranit Nik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537417/
https://www.ncbi.nlm.nih.gov/pubmed/28381879
http://dx.doi.org/10.1038/jhg.2017.37

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537417/
https://www.ncbi.nlm.nih.gov/pubmed/28381879
http://dx.doi.org/10.1038/jhg.2017.37

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