Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.
about
Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review.The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms.ATP13A2 variability in Taiwanese Parkinson's disease.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).Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9).
P2860
Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Lack of association between AT ...... population of mainland China.
@en
Lack of association between AT ...... population of mainland China.
@nl
type
label
Lack of association between AT ...... population of mainland China.
@en
Lack of association between AT ...... population of mainland China.
@nl
prefLabel
Lack of association between AT ...... population of mainland China.
@en
Lack of association between AT ...... population of mainland China.
@nl
P2093
P1433
P1476
Lack of association between AT ...... population of mainland China.
@en
P2093
Hai-Yan Zhou
Qing-Zhou Fei
Ting Zhang
Xi-Jin Wang
P356
10.1016/J.NEULET.2010.03.018
P407
P577
2010-03-19T00:00:00Z