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De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

författare

Maria Martinez

Françoise Clerget-Darpoux

publicerad i: Journal of Medical Genetics

utgivningsår: 1998-08-01

språk: engelska

huvudämne: Alzheimers sjukdom

Refererar artiklar 11

Datum

Titel

Författare

1997-01-01

Assignment of Alzheimer's presenilin-2 (PS-2) gene to 1q42.1 by fluorescence in situ hybridization
1996-01-01

The gene defects responsible for familial Alzheimer's disease

Robert D. Moir
1996-11-01

Sequence analysis of presenilin-1 gene mutation in Japanese Alzheimer's disease patients.
1996-08-01

Missense mutations of the PS-1/S182 gene in German early-onset Alzheimer's disease patients.

Hans Förstl
1996-07-08

A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years

Yves Agid
1995-12-01

A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene
1995-12-01

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease
1995-08-01

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
1995-08-18

Candidate gene for the chromosome 1 familial Alzheimer's disease locus
1995-06-29

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Jonathan L Haines
1984-07

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease,Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group* under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

Artikel - wd:Q33681141

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