Frequency of frontotemporal dementia gene variants in C9ORF72, MAPT, and GRN in academic versus commercial laboratory cohorts

BACKGROUND: Frontotemporal lobar degeneration (FTLD) is a leading cause of dementia, and elucidating its genetic underpinnings is critical. FTLD research centers typically recruit patient cohorts that are limited by the center’s specialty and the ways in which its geographic location affects the eth...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Adv Genomics Genet
Hlavní autoři: Steele, Natasha ZR, Bright, Alison R, Lee, Suzee E, Fong, Jamie C, Bonham, Luke W, Karydas, Anna, Karbassi, Izabela D, Pribadi, Mochtar, Meservey, Marc A, Gallen, Matthew C, Ramos, Eliana Marisa, Liaquat, Khalida, Hoffman, Carol C, Krasner, Meagan R, Dodge, Whitney, L Miller, Bruce, Coppola, Giovanni, Rankin, Katherine P, Yokoyama, Jennifer S, Higgins, Joseph J
Médium: Artigo
Jazyk:Inglês
Vydáno: 2018
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6483103/
https://ncbi.nlm.nih.gov/pubmed/31031559
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/AGG.S164047
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky