Caricamento...
MAPT haplotype diversity in multiple system atrophy
INTRODUCTION: Multiple system atrophy (MSA) is a rare progressive neurodegenerative disorder. MSA was originally considered exclusively sporadic but reports of association with genes such as SNCA, COQ2 and LRRK2 have demonstrated that there is a genetic contribution to the disease. MAPT has been ass...
Salvato in:
| Pubblicato in: | Parkinsonism Relat Disord |
|---|---|
| Autori principali: | , , , , , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2016
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5007155/ https://ncbi.nlm.nih.gov/pubmed/27374978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2016.06.010 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|