The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
about
Parkinson's disease: from monogenic forms to genetic susceptibility factorsLeucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration.Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritanceG2385R and I2020T Mutations Increase LRRK2 GTPase ActivityIdentification of a Japanese family with LRRK2 p.R1441G-related Parkinson's diseaseLeucine-rich repeat kinase 2 (LRRK2): a key player in the pathogenesis of Parkinson's diseaseLRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population.Genetics of Parkinson's disease: LRRK2 on the rise.Lrrk2 mutations in South America: A study of Chilean Parkinson's disease.Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort.Analysis of the LRRK2 p.G2019S mutation in Colombian Parkinson's Disease Patients.Parkinson's disease: the genetics of a heterogeneous disorder.P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population.Genetics of Parkinson disease.Mutations in LRRK2 as a cause of Parkinson's disease.The G2019S LRRK2 Mutation is Rare in Korean Patients with Parkinson's Disease and Multiple System AtrophyLRRK2 in Parkinson's disease: genetic and clinical studies from patients.Genetic basis of Parkinson's disease: inheritance, penetrance, and expression.Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson's Disease.LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.Pathogenicity of LRRK2 P755L variant in Parkinson's disease.The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson's disease.Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson's disease.Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease.LRRK 2 gene mutations in the pathophysiology of the ROCO domain and therapeutic targets for Parkinson's disease: a review.
P2860
Q22242870-8752D3BA-7BBA-40A7-9CE0-6580BD2AF7EBQ24298689-44F7C7BE-53B3-4FDA-9188-8653AB0602FDQ28077356-EE0ED21E-D00E-4D9E-80F1-9877652FBFC3Q29347540-74AD9FC7-8C59-4667-AF46-C270DEB2251BQ30587398-ABA91955-04B2-4B28-9C0F-56A6FE5D220DQ33812599-8A5D2364-EC8D-4188-928B-05AC86DEBAB0Q34177234-21B1ACE4-A5C9-459E-BF6B-6EE3B24A3CC1Q34470633-F9AE6685-7D3C-41CB-AFD2-17B6CA404479Q36002998-9BC14839-1EC7-4EA9-B0FF-21360B204290Q36226461-344B2387-AB9C-428A-BABA-8F11E8A63ABDQ36267736-830A3EA4-E496-4567-9552-3E07FAD02D93Q36516918-A283B058-2F88-455F-B26A-ECCDB9ABF056Q36871156-FAA1CE84-3386-4546-94E0-C9C60F65D785Q37037053-3E899BD9-E45B-41F0-8C94-5D691BB5F2DCQ37039473-6FF56797-28DA-413A-B0D1-2C8AB1C5FCA0Q37203387-6C1DC89D-0E8A-4ED9-AFA5-BCA45F2DAEA9Q37608624-6FD0029F-03ED-4A41-BB5E-B413EBBF0C28Q38115298-37CB9E83-171D-4BD9-AE17-61A9243E94B4Q38738200-A8EFC2C9-B63B-483B-9E4F-02500802D94BQ40133563-2962C37D-1B4D-4638-B5FA-E06CFECA57C3Q42675021-A3AD79B2-E524-4D16-A799-14D11578849BQ44149214-78E498A2-82BA-45A5-B117-CBA00A405AF9Q44594403-F60B1F29-05CC-4085-B7E8-A03594E7C4ABQ46791050-F4D5F01E-C8D8-4B9F-934B-80AC0476A99EQ54571312-60FD61B8-4EE1-4ADD-8135-A1B7D09871E6Q55410950-8BF5E015-408E-4588-9C18-3059A0587529
P2860
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
@en
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
@nl
type
label
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
@en
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
@nl
prefLabel
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
@en
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
@nl
P2093
P50
P1433
P1476
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
@en
P2093
Jian-Jun Liu
P304
P356
10.1016/J.NEULET.2005.04.103
P407
P577
2005-08-01T00:00:00Z