Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
about
Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review.The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms.The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).Developmental expression of P5 ATPase mRNA in the mouse.
P2860
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@en
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@nl
type
label
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@en
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@nl
altLabel
Genetic association study of the P-type ATPaseATP13A2in late-onset Parkinson's disease
@en
prefLabel
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@en
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@nl
P2093
P2860
P50
P356
P1433
P1476
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
@en
P2093
Aleksandar Rakovic
Ana Djarmati
Antonia Flaquer
Barbara Stiller
Christian Kubisch
Jan Freudenberg
Katja Lohmann
Michael Linnebank
Mohammad-Reza Toliat
Sebastian Paus
P2860
P304
P356
10.1002/MDS.22399
P407
P577
2009-02-01T00:00:00Z