Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions-Reference-Cited by-同舟云学术

Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions

Published:2014-11 Issue:11 Volume:35 Page:2658.e1-2658.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Lattante Serena,Le Ber Isabelle,Galimberti Daniela,Serpente Maria,Rivaud-Péchoux Sophie,Camuzat Agnès,Clot Fabienne,Fenoglio Chiara,Scarpini Elio,Brice Alexis,Kabashi Edor

Funder

Atip/Avenir

Inserm

Career Integration Grant

Robert Packard Foundation

AFM

ARSLA

Fondation Cognacq-Jay

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference21 articles.

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3. TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways;Chen-Plotkin;J. Neurosci.,2012

4. Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels;Cruchaga;Arch. Neurol.,2011

5. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;DeJesus-Hernandez;Neuron,2011

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