Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation

BACKGROUND: Mutations of the Ectodysplasin-A (EDA) gene are generally associated with syndrome hypohidrotic ectodermal dysplasia or nonsyndromic tooth agenesis. The influence of EDA mutations on dentinogenesis and odontoblast differentiation has not been reported. The aim of this study was to identi...

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Detalles Bibliográficos
Autores principales: Pan, Yuhua, Lu, Ting, Peng, Ling, Zeng, Qi, Huang, Xiangyu, Yao, Xinchen, Wu, Buling, Xiong, Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449729/
https://www.ncbi.nlm.nih.gov/pubmed/34545288
http://dx.doi.org/10.1155/2021/7653013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449729/
https://www.ncbi.nlm.nih.gov/pubmed/34545288
http://dx.doi.org/10.1155/2021/7653013

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