Carregant...
A novel exon 2 I27V valosin-containing protein variant is associated with dissimilar clinical syndromes
Mutations in valosin-containing protein (VCP) are associated with a syndromic constellation of inclusion body myositis, Paget’s disease of bone and frontotemporal dementia. Here we describe the case reports of two patients with a novel variation (p.I27V) in the VCP gene that was not identified in a...
Guardat en:
| Publicat a: | J Neurol |
|---|---|
| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4606971/ https://ncbi.nlm.nih.gov/pubmed/21387114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-011-5966-4 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|