Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement-Reference-Cited by-同舟云学术

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Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

Published:2013-01-01 Issue:1 Volume:70 Page:78
ISSN:2168-6149
Container-title:JAMA Neurology
language:en
Short-container-title:JAMA Neurol

Author:

Guerreiro Rita João,Lohmann Ebba,Brás José Miguel,Gibbs Jesse Raphael,Rohrer Jonathan D.,Gurunlian Nicole,Dursun Burcu,Bilgic Basar,Hanagasi Hasmet,Gurvit Hakan,Emre Murat,Singleton Andrew,Hardy John

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology

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1. Alterations in the Brain Lipidome of Alzheimer’s Disease Donors with Rare TREM2 Risk Variants;2024-08-22

2. Multimerization of TREM2 is impaired by Alzheimer's disease–associated variants;Alzheimer's & Dementia;2024-07-20

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4. Current understanding on TREM-2 molecular biology and physiopathological functions;International Immunopharmacology;2024-06

5. Homozygous TREM2 c.549del; p.(Leu184Serfs*5) variant causing Nasu‐Hakola disease in three siblings in a consanguineous Iraqi family: Case report and review of literature;Molecular Genetics & Genomic Medicine;2024-06

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