Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

OBJECTIVE: The genetic risk architecture of Alzheimer disease (AD) is complex with single pathogenic mutations leading to early-onset AD, while both rare and common genetic susceptibility variants contribute to the more widespread late-onset AD (LOAD); we sought to discover novel genes contributing...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Neurol Genet
Egile Nagusiak: Kohli, Martin A., Cukier, Holly N., Hamilton-Nelson, Kara L., Rolati, Sophie, Kunkle, Brian W., Whitehead, Patrice L., Züchner, Stephan L., Farrer, Lindsay A., Martin, Eden R., Beecham, Gary W., Haines, Jonathan L., Vance, Jeffery M., Cuccaro, Michael L., Gilbert, John R., Schellenberg, Gerard D., Carney, Regina M., Pericak-Vance, Margaret A.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Wolters Kluwer 2016
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4817909/
https://ncbi.nlm.nih.gov/pubmed/27066578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000041
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