Oral and Craniofacial Manifestations and Two Novel Missense Mutations of the NTRK1 Gene Identified in the Patient with Congenital Insensitivity to Pain with Anhidrosis

Congenital insensitivity to pain with anhidrosis (CIPA) is a rare inherited disorder of the peripheral nervous system resulting from mutations in neurotrophic tyrosine kinase receptor 1 gene (NTRK1), which encodes the high-affinity nerve growth factor receptor TRKA. Here, we investigated the oral an...

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Detalles Bibliográficos
Autores principales: Gao, Li, Guo, Hao, Ye, Nan, Bai, Yudi, Liu, Xin, Yu, Ping, Xue, Yang, Ma, Shufang, Wei, Kewen, Jin, Yan, Wen, Lingying, Xuan, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682965/
https://www.ncbi.nlm.nih.gov/pubmed/23799134
http://dx.doi.org/10.1371/journal.pone.0066863

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682965/
https://www.ncbi.nlm.nih.gov/pubmed/23799134
http://dx.doi.org/10.1371/journal.pone.0066863

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