SNCA And NotM. J. Farrer

List of bibliographic references

Number of relevant bibliographic references: 6.

Ident.	Authors (with country if any)	Title
000162	Eugénie Mutez [France] ; Frédéric Leprêtre [France] ; Emilie Le Rhun [France] ; Lydie Larvor [France] ; Aurélie Duflot [France] ; Vincent Mouroux [France] ; Jean-Pierre Kerckaert [France] ; Martin Figeac [France] ; Kathy Dujardin [France] ; Alain Destée [France] ; Marie-Christine Chartier-Harlin [France]	SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes
000493	Haydeh Payami [États-Unis] ; Denise M. Kay [États-Unis] ; Cyrus P. Zabetian [États-Unis] ; Gerard D. Schellenberg [États-Unis] ; Stewart A. Factor [Géorgie (pays)] ; Colin C. Mcculloch [États-Unis]	Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease
000704	Karen Nuytemans [Belgique] ; Jessie Theuns [Belgique] ; Marc Cruts [Belgique] ; Christine Van Broeckhoven [Belgique]	Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
000822	Gerassimos E. Voutsinas [Grèce] ; Eleana F. Stavrou [Grèce] ; Gerassimos Karousos [Grèce] ; Aggeliki Dasoula [Grèce] ; Adamantia Papachatzopoulou [Grèce] ; Maria Syrrou [Grèce] ; Annemieke J. M. H. Verkerk [Pays-Bas] ; Peter Van Der Spek [Pays-Bas] ; George P. Patrinos [Pays-Bas, Grèce] ; Reinhard Stöger [États-Unis, Royaume-Uni] ; Aglaia Athanassiadou [Grèce]	Allelic imbalance of expression and epigenetic regulation within the alpha‐synuclein wild‐type and p.Ala53Thr alleles in Parkinson disease
000A86	Sarah Teixeira Camargos [Brésil] ; Leonardo Oliveira Dornas [Brésil] ; Parastoo Momeni [États-Unis] ; Andrew Lees (neurologue) [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Andrew Singleton [États-Unis] ; Francisco Cardoso [Brésil]	Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations
000E71	E. V. De Marco [Italie] ; P. Tarantino [Italie] ; F. E. Rocca [Italie] ; G. Provenzano [Italie] ; D. Civitelli [Italie] ; V. De Luca [Italie] ; F. Annesi [Italie] ; S. Carrideo [Italie] ; I. C. Cir Candiano [Italie] ; N. Romeo [Italie] ; G. Nicoletti [Italie] ; R. Marconi [Italie] ; F. Novellino [Italie] ; M. Morelli [Italie] ; A. Quattrone [Italie] ; G. Annesi [Italie]	Alpha‐synuclein promoter haplotypes and dementia in Parkinson's Disease

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