New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

about

DnaJ/Hsp40 Family and Parkinson's Disease.Astrocytes, Microglia, and Parkinson's Disease.

P2860

Q49233227-4EB47336-F8AB-4B6C-B945-21B73FC8D445 Q55000928-F97EF12F-DCDE-412A-9821-A2FF30D80973

P2860

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

Item

http://www.wikidata.org/entity/Q39451649

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

@en

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

@nl

type

Item

label

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

@en

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

@nl

prefLabel

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

@en

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

@nl

P1476

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism

@en

P2093

Andreas Puschmann

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

P275

Creative Commons Attribution

P2860

A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism

Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

Identification of TMEM230 mutations in familial Parkinson's disease

Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism

Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications

DNAJC13 mutations in Parkinson disease

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.

Genetics of Parkinson's disease.

P2888

s11910-017-0780-8

P304

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

P31

scholarly article

P356

10.1007/S11910-017-0780-8

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

P433

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

P478

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

P50

Andreas Puschmann

P5008

ScienceSource

P577

2017-09-01T00:00:00Z

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

P698

28733970

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

P921

Parkinson's disease

genetic variation

P932

5522513

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

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

about

P2860

P2860

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

description

name

type

label

prefLabel

P1433

P1476

P2093

P275

P2860

P2888

P304

P31

P356

P433

P478

P50

P5008

P577

P698

P921

P932

P356

P1433

P1476

P2093

P275

P2860

P2888

P304

P31

P356

P433

P478

P50

P5008

P577

P698

P921

P932