The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients-Reference-Cited by-同舟云学术

The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients

Published:1996-12 Issue:6 Volume:40 Page:912-917
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Ikeda Masaki,Sharma Vikram,Mark Sumi S.,Rogaeva Ekaterina A.,Poorkaj Parvoneh,Sherrington Robin,Nee Linda,Tsuda Takehide,Oda Nobuhito,Watanabe Mitsunori,Aoki Masashi,Shoji Mikio,Abe Koji,Itoymia Yasuto,Hirai Shurisaku,Schellenberg Gerard D.,Bird Thomas D.,George-Hyslop P. H. St

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference16 articles.

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

2. A Familial Alzheimer's Disease Locus on Chromosome 1

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

4. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant

5. Presenilins and Alzheimer disease

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