Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased A 42 Secretion-Reference-Cited by-同舟云学术

Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased A 42 Secretion

Published:1999-08-01 Issue:8 Volume:8 Page:1529-1540
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

De Jonghe C.,MarcCruts ,Rogaeva E. A.,Tysoe C.,Singleton A.,Vanderstichele H.,Meschino W.,Dermaut B.,Vanderhoeven I.,Backhovens H.,Vanmechelen E.,Morris C. M.,Hardy J.,Rubinsztein D. C.,St George-Hyslop P. H.,Van Broeckhoven C.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/8/8/1529/1657630/8-8-1529.pdf

Reference57 articles.

1. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

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

3. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus

4. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

5. Presenilin mutations in Alzheimer's disease

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