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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 4, 2024. (Total: 232145Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Dementia and CREBBP[original query]
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.
Journal of human genetics 2006 51 (8): 645-51.
Costa Maria do Carmo, Teixeira-Castro Andreia, Constante Marco, Magalhães Marina, Magalhães Paula, Cerqueira Joana, Vale José, Passão Vitorina, Barbosa Célia, Robalo Conceição, Coutinho Paula, Barros José, Santos Manuela M, Sequeiros Jorge, Maciel Patríc
Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease.
Neurology. Genetics 2017 Oct 3 (5): e178.
Vardarajan Badri N, Tosto Giuseppe, Lefort Roger, Yu Lei, Bennett David A, De Jager Philip L, Barral Sandra, Reyes-Dumeyer Dolly, Nagy Peter L, Lee Joseph H, Cheng Rong, Medrano Martin, Lantigua Rafael, Rogaeva Ekaterina, St George-Hyslop Peter, Mayeux Richa
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