Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study. - Wikidata - awgldk - TriplyDB

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.

http://www.wikidata.org/entity/Q33183359

about

Genetics of Parkinson's disease: LRRK2 on the rise.The genetics of Parkinson disease.The genetic basis of Parkinson's disease Imaging synucleinopathies.Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population.Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).Accumulation and distribution of α-synuclein and ubiquitin in the CNS of Gaucher disease mouse models Genetics of Parkinson's disease

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P2860

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.

http://www.wikidata.org/entity/Q33183359

description

2002 nî lūn-bûn

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2002 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի հունվարին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

Two large British kindreds wit ...... athological and genetic study.

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Two large British kindreds wit ...... athological and genetic study.

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Two large British kindreds wit ...... athological and genetic study.

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Two large British kindreds wit ...... athological and genetic study.

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Two large British kindreds wit ...... athological and genetic study.

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Two large British kindreds wit ...... athological and genetic study.

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Two large British kindreds wit ...... athological and genetic study.

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A C Williams

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D E W Aldous

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D J Brooks

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D J Nicholl

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G G Lennox

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J R Vaughan

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M Farrer

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N L Khan

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P2860

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

Lewy bodies and parkinsonism in families with parkin mutations

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

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

Association between early-onset Parkinson's disease and mutations in the parkin gene

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44-57

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scholarly article

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10.1093/BRAIN/AWF013

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P433

Pt 1

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125

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2002-01-01T00:00:00Z

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277387074

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11834592

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