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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

http://www.wikidata.org/entity/Q35067666

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Association of LRRK2 R1628P variant with Parkinson's disease in Ethnic Han-Chinese and subgroup population.Relationship between LRRK2 R1628P polymorphism and Parkinson's disease in Asian populations.Efficient identification of SNPs in pooled DNA samples using a dual mononucleotide addition-based sequencing method.Genetic Analysis of LRRK2 R1628P in Parkinson's Disease in Asian Populations.The genetic architecture of mitochondrial dysfunction in Parkinson's disease.Haplotype-Contained PCR Products Analysis by Sequencing with Selective Restriction of Primer Extension.LRRK 2 gene mutations in the pathophysiology of the ROCO domain and therapeutic targets for Parkinson's disease: a review.

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P2860

Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

http://www.wikidata.org/entity/Q35067666

description

2013 nî lūn-bûn

@nan

2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

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JOURNAL.PONE.0082001

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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease

@en

P2093

Bo-Hsun Lee

http://www.w3.org/2001/XMLSchema#string

Chih-Ying Chao

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Chiung-Mei Chen

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Fen-Ju Hu

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Guey-Jen Lee-Chen

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Hsuan-Chu Hsu

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Kuo-Hsuan Chang

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Pei-Ru Jiang

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Wan-Ling Chen

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Wen-Teng Chang

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P2860

Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

The G2385R variant of leucine-rich repeat kinase 2 associated with Parkinson's disease is a partial loss-of-function mutation

The kinase LRRK2 is a regulator of the transcription factor NFAT that modulates the severity of inflammatory bowel disease

Consensus-derived structural determinants of the ankyrin repeat motif

Genome-wide association study reveals genetic risk underlying Parkinson's disease

A New Statistical Method for Haplotype Reconstruction from Population Data

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

LRRK2 in Parkinson's disease: protein domains and functional insights

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

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e82001

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Parkinson's disease

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