A rare missense variant in CASP7 is associated with familial late-onset Alzheimer disease

INTRODUCTION: The genetic architecture of Alzheimer disease (AD) is only partially understood. METHODS: We conducted an association study for AD using whole sequence data from 507 genetically enriched AD cases (i.e., cases having close relatives affected by AD) and 4,917 cognitively healthy controls...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Alzheimers Dement
Asıl Yazarlar: Zhang, Xiaoling, Zhu, Congcong, Beecham, Gary, Vardarajan, Badri N., Ma, Yiyi, Lancour, Daniel, Farrell, John J., Chung, Jaeyoon, Mayeux, Richard, Haines, Jonathan L., Schellenberg, Gerard D., Pericak-Vance, Margaret A., Lunetta, Kathryn L, Farrer, Lindsay A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2019
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6408965/
https://ncbi.nlm.nih.gov/pubmed/30503768
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jalz.2018.10.005
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller