Mutation analysis of patients with neurodegenerative disorders using NeuroX array-Reference-Cited by-同舟云学术

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Mutation analysis of patients with neurodegenerative disorders using NeuroX array

Published:2015-01 Issue:1 Volume:36 Page:545.e9-545.e14
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Ghani Mahdi,Lang Anthony E.,Zinman Lorne,Nacmias Benedetta,Sorbi Sandro,Bessi Valentina,Tedde Andrea,Tartaglia Maria Carmela,Surace Ezequiel I.,Sato Christine,Moreno Danielle,Xi Zhengrui,Hung Rachel,Nalls Mike A.,Singleton Andrew,St George-Hyslop Peter,Rogaeva Ekaterina

Funder

Canadian Institutes of Health Research

Ontario Research Fund

the W. Garfield Weston Foundation

National Institute on Aging

National Institutes of Health

Department of Health and Human Services

Cassa di Risparmio di Pistoia e Pescia

Cassa di Risparmio di Firenze

Ministry of Health

PRIN

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference40 articles.

1. Use of haptoglobin and transthyretin as potential biomarkers for the preclinical diagnosis of Parkinson's disease;Arguelles;Neurochem. Int.,2010

2. G41S SOD1 mutation: a common ancestor for six ALS Italian families with an aggressive phenotype;Battistini;Amyotroph. Lateral Scler.,2010

3. TREM2 and neurodegenerative disease;Benitez;N. Engl. J. Med.,2013

4. Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk;Bettens;Mol. Neurodegener.,2012

5. TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis;Cady;JAMA Neurol.,2014

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