A carregar...
Hereditary sensory and autonomic neuropathy type V: Report of a rare case
Hereditary sensory and autonomic neuropathy (HSAN) type V is a rare inherited disease caused by a mutation in the neurotrophic tyrosine kinase receptor, type 1 gene located on chromosome 1 (1q21-q22). It is characterized by pain insensitivity, partial anhydrosis without mental retardation and unimpa...
Na minha lista:
| Publicado no: | Contemp Clin Dent |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4319325/ https://ncbi.nlm.nih.gov/pubmed/25684922 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.149302 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|