Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis

Both X-linked hypohidrotic ectodermal dysplasia (XLHED) and non-syndromic tooth agenesis (NSTA) result in symptoms of congenital tooth loss. This study investigated genetic causes in two families with XLHED and four families with NSTA. We screened for mutations of WNT10A, EDA, EDAR, EDARADD, PAX9, M...

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Detalles Bibliográficos
Autores principales: Zeng, Binghui, Zhao, Qi, Li, Sijie, Lu, Hui, Lu, Jiaxuan, Ma, Lan, Zhao, Wei, Yu, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664109/
https://www.ncbi.nlm.nih.gov/pubmed/28981473
http://dx.doi.org/10.3390/genes8100259

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664109/
https://www.ncbi.nlm.nih.gov/pubmed/28981473
http://dx.doi.org/10.3390/genes8100259

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