Influence of low frequency PSEN1 variants on familial Alzheimer’s disease risk in Brazil-Reference-Cited by-同舟云学术

Influence of low frequency PSEN1 variants on familial Alzheimer’s disease risk in Brazil

Published:2017-07 Issue: Volume:653 Page:341-345
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Abdala Bianca Barbosa,dos Santos Jussara Mendonça,Gonçalves Andressa Pereira,da Motta Luciana Branco,Laks Jerson,de Borges Margarete Borges,Gonçalves Pimentel Márcia Mattos,Santos-Rebouças Cíntia Barros

Funder

Ministério da Saúde (MS/Brazil)

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ/Brazil)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq/Brazil)

CEPUERJ

Publisher

Elsevier BV

Subject

General Neuroscience

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4. Estimation of the genetic contribution of presenilin-1 and –2 mutations in a population-based study of presenile Alzheimer disease;Cruts;Hum. Mol. Genet.,1998

5. Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations;Rogaeva;Neurology,2001

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1. Patient with PSEN1 Glu318Gly and Other Possible Disease Risk Mutations, Diagnosed with Early Onset Alzheimer’s Disease;International Journal of Molecular Sciences;2023-10-23

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3. Genetics, Functions, and Clinical Impact of Presenilin-1 (PSEN1) Gene;International Journal of Molecular Sciences;2022-09-19

4. Italian Case Report with a Double Mutation in PSEN1 (K311R and E318G);Neurology International;2022-05-16

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