Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism

BACKGROUND: Parkinson's disease is a progressive neurodegenerative disorder, where most cases are sporadic with a late onset. In rare incidences familial forms of early-onset parkinsonism occur, and when recessively inherited, cases are often explained by mutations in either the parkin (PARK2)...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Myhre, Ronny, Steinkjer, Stina, Stormyr, Alice, Nilsen, Gina L, Zayyad, Hiba Abu, Horany, Khalid, Nusier, Mohamad K, Klungland, Helge
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2008
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2635385/
https://ncbi.nlm.nih.gov/pubmed/19087301
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-8-47
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars