Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

Item
http://www.wikidata.org/entity/Q24539105
Parkinson's disease-associated kinase PINK1 regulates Miro protein level and axonal transport of mitochondriaHow much phenotypic variation can be attributed to parkin genotype?PARK2 mediates interleukin 6 and monocyte chemoattractant protein 1 production by human macrophages.The genetics of Parkinson disease.Genetic testing in Parkinson's disease.Analysis of PRKN Variants and Clinical Features in Polish Patients with Parkinson's DiseaseParkinson's disease in Arabs: a systematic review.A multidisciplinary study of patients with early-onset PD with and without parkin mutations.Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.Parkin expression in the adult mouse brain.Merging mouse transcriptome analyses with Parkinson's disease linkage studies.Genetic epidemiology of Parkinson's disease.Juvenile parkinsonism: a heterogeneous entity.Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease.Involvement of spinal motor neurons in parkin-positive autosomal recessive juvenile parkinsonism.A susceptibility gene for late-onset idiopathic Parkinson's diseaseAssessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics
P2860

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

Item
http://www.wikidata.org/entity/Q24539105
description
1998 nî lūn-bûn
@nan
1998 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@ast
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@en
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@nl
type
label
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@ast
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@en
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@nl
altLabel
Chromosome 6–Linked Autosomal ...... ozygous Deletion in One Family
@en
prefLabel
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@ast
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@en
Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
@nl
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Chromosome 6-linked autosomal ...... inson's Disease Genetics Study
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P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P5875
P698
P921
P932