A carregar...
RFLP analysis for APP 717 mutations associated with Alzheimer's disease.
Familial Alzheimer's disease (FAD) has been shown to be associated with three distinct point mutations within the same codon of the amyloid precursor protein (APP) gene. The mutation identified in the Indiana kindred is a G-->T transversion at the first position of the codon for amino acid 7...
Na minha lista:
| Publicado no: | J Med Genet |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1993
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016419/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7686976/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.6.476 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|