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Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder, characterized by loss of algesthesis and inability to sweat. CIPA is known to be caused by mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1). However, the details of NTRK1 mutatio...
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| Publicado no: | Mol Pain |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6009080/ https://ncbi.nlm.nih.gov/pubmed/29770739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1744806918781140 |
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