Genetic causes of Parkinson’s disease in the Maltese: a study of selected mutations in LRRK2, MTHFR, QDPR and SPR

BACKGROUND: Mutations in Leucine-rich repeat kinase 2 NM_198578 (LRRK2 c.6055G > A (p.G2019S), LRRK2 c.4321C > G (p.R1441G)) and alpha-synuclein NM_000345 (SNCA c.209G > A (p.A53T)) genes causing Parkinson’s disease (PD) are common in Mediterranean populations. Variants in the Quinoid Dihyd...

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Bibliografiska uppgifter
I publikationen:BMC Med Genet
Huvudupphovsmän: Zahra, Charmaine, Tabone, Christine, Camilleri, Graziella, Felice, Alex E., Farrugia, Rosienne, Bezzina Wettinger, Stephanie
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2016
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5016953/
https://ncbi.nlm.nih.gov/pubmed/27613114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0327-x
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