Carregant...
Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington’s Disease Knock-In Mice
Huntington’s disease (HD) is a neurodegenerative disorder caused by the expansion of a CAG trinucleotide repeat in exon 1 of the HTT gene. Longer repeat sizes are associated with increased disease penetrance and earlier ages of onset. Intergenerationally unstable transmissions are common in HD famil...
Guardat en:
| Publicat a: | Genetics |
|---|---|
| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Genetics Society of America
2017
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5289832/ https://ncbi.nlm.nih.gov/pubmed/27913616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.116.195578 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|