A carregar...
Novel GRN Mutations in Patients with Corticobasal Syndrome
Loss-of-function GRN mutations lead to GRN haploinsufficiency and consequently neurodegeneration with significant heterogeneity in clinical presentation of various syndromes. The aim of this study was to investigate the genetics and clinical features of patients with GRN-related frontotemporal lobar...
Na minha lista:
| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4785496/ https://ncbi.nlm.nih.gov/pubmed/26961809 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep22913 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|