Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS-Reference-Cited by-同舟云学术

Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS

Published:2020-04-26 Issue:5-6 Volume:21 Page:470-472
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Sokratous Maria¹,Lucia Schottlaender²,Bourinaris Thomas³,Marogianni Chrysoula¹,Arnaoutoglou Marianthi⁴,Patrikiou Eleni⁵,Ralli Styliani¹,Markou Aikaterini¹,Dardiotis Efthimios¹,Houlden Henry³,Hadjigeorgiou Georgios M.¹⁶,Xiromerisiou Georgia¹

Affiliation:

1. Faculty of Medicine School of Health Sciences, Department of Neurology, University Hospital of Larissa, University of Thessaly, Larissa, Greece,

2. Argentine National Scientific and Technological Research Council (CONICET), FLENI Neurological Research Institute, Buenos Aires, Argentina,

3. Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK,

4. First Neurology Clinic, AHEPA Hospital, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece,

5. Faculty of Medicine, Department of Rheumatology and Clinical Immunology, School of Health Sciences, University of Thessaly, Larisa, Greece, and

6. Department of Neurology, Medical School, University of Cyprus, Nicosia, Cyprus

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2020.1757115

Reference10 articles.

1. Staging amyotrophic lateral sclerosis: A new focus on progression

2. Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

3. The role of C9orf72 in neurodegenerative disorders: a systematic review, an updated meta-analysis, and the creation of an online database

4. High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients

5. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

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