Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

about

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

Item

http://www.wikidata.org/entity/Q57072461

description

wetenschappelijk artikel

@nl

наукова стаття, опублікована у 2018

@uk

name

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@en

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@nl

type

Item

label

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@en

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@nl

altLabel

Clinical Heterogeneity Among LRRK2 Variants in Parkinson's Disease: A Meta-Analysis

@en

Clinical Heterogeneity Among

@en

prefLabel

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@en

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@nl

P1476

Clinical Heterogeneity Among Variants in Parkinson's Disease: A Meta-Analysis

@en

P2093

Beisha Tang

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

Hongxu Pan

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

Jifeng Guo

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

Li Shu

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

Qian Xu

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

Qiying Sun

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

Yuan Zhang

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

P2860

Categorization of humans in biomedical research: genes, race and disease

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan

LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients.

Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data.

LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease

Clinical correlates of depressive symptoms in familial Parkinson's disease.

P304

283

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

P31

scholarly article

P356

10.3389/FNAGI.2018.00283

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

P4011

30f368acda467446b731be2a73adde32ca41617a

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

P407

English

P478

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

P577

2018-01-01T00:00:00Z

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

P698

30283330

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

P921

Parkinson's disease

Ageing

P932

6156433

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