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

The presenilin 1 (PS1) gene, located on chromosome 14, is the major gene involved in the autosomal dominant forms of early onset Alzheimer's disease (AD). In order to estimate the frequency of de novo PS1 mutations, we have sequenced the PS1 open reading frame in 13 clinically diagnosed patient...

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Main Authors: Dumanchin, C, Brice, A, Campion, D, Hannequin, D, Martin, C, Moreau, V, Agid, Y, Martinez, M, Clerget-Darpoux, F, Frebourg, T
格式: Artigo
語言:Inglês
出版: 1998
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051395/
https://ncbi.nlm.nih.gov/pubmed/9719376
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