Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia-Reference-Cited by-同舟云学术

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia

Published:2019-01-08 Issue:1 Volume:67 Page:159-167
ISSN:1387-2877
Container-title:Journal of Alzheimer's Disease
language:
Short-container-title:JAD

Author:

Guven Gamze¹,Bilgic Başar²,Tufekcioglu Zeynep²,Erginel Unaltuna Nihan¹,Hanagasi Hasmet²,Gurvit Hakan²,Singleton Andrew³,Hardy John⁴,Emre Murat²,Gulec Cagri⁵,Bras Jose⁴⁶⁷,Guerreiro Rita⁴⁶⁷,Lohmann Ebba⁸⁹

Affiliation:

1. Department of Genetics, Aziz Sancar Institute for Experimental Medicine, Istanbul University, Istanbul, Turkey

2. Department of Neurology, Behavioural Neurology and Movement Disorders Unit, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey

3. Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA

4. Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK

5. Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey

6. Department of Medical Sciences and Institute of Biomedicine – iBiMED, University of Aveiro, Aveiro, Portugal

7. UK Dementia Research Institute at UCL (UK DRI), London, UK

8. Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Germany

9. DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

Reference32 articles.

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3. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21;Cruts;Nature,2006

4. A novel splice-acceptor site mutation in GRN (c.709-2 A>T) causes frontotemporal dementia spectrum in a large family from Southern Italy;Sassi;J Alzheimers Dis,2016

5. Manic behavior and asymmetric right frontotemporal dementia from a novel progranulin mutation;Mendez;Neuropsychiatr Dis Treat,2018

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