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

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Title: Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.
Authors: Mitropoulos K; National and Kapodistrian University of Athens School of Medicine, Athens, Greece., Merkouri Papadima E; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Xiromerisiou G; School of Medicine, University of Thessaly, Larisa, Greece., Balasopoulou A; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Charalampidou K; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Galani V; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Zafeiri KV; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Dardiotis E; School of Medicine, University of Thessaly, Larisa, Greece., Ralli S; School of Medicine, University of Thessaly, Larisa, Greece., Deretzi G; Papageorgiou hospital, Thessaloniki, Greece., John A; Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, UAE., Kydonopoulou K; ANALYSI Diagnostic Laboratories S.A, Thessaloniki, Greece., Papadopoulou E; ANALYSI Diagnostic Laboratories S.A, Thessaloniki, Greece., di Pardo A; Departments of Neurology and Physiology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Akcimen F; Suna and Inan Kirac Foundation, NDAL, Bogazici University, Istanbul, Turkey., Loizedda A; Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.; CNR IRGB, Cagliari, Italy., Dobričić V; Institute of Neurology CCS, School of Medicine, University of Belgrade, Belgrade, Serbia., Novaković I; Institute of Neurology CCS, School of Medicine, University of Belgrade, Belgrade, Serbia.; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, Belgrade, Serbia., Kostić VS; Institute of Neurology CCS, School of Medicine, University of Belgrade, Belgrade, Serbia., Mizzi C; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Peters BA; Complete Genomics Inc., Mountain View, CA, USA.; BGI Shenzhen, Shenzhen, People's Republic of China., Basak N; Suna and Inan Kirac Foundation, NDAL, Bogazici University, Istanbul, Turkey., Orrù S; Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy., Kiskinis E; Departments of Neurology and Physiology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Cooper DN; Institute of Medical Genetics, Cardiff University, Cardiff, UK., Gerou S; ANALYSI Diagnostic Laboratories S.A, Thessaloniki, Greece., Drmanac R; Complete Genomics Inc., Mountain View, CA, USA., Bartsakoulia M; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Tsermpini EE; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Hadjigeorgiou GM; School of Medicine, University of Thessaly, Larisa, Greece., Ali BR; Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, UAE., Katsila T; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece., Patrinos GP; Department of Pharmacy, University of Patras School of Health Sciences, Campus, Rion, GR-26504, Patras, Greece. gpatrinos@upatras.gr.; Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, UAE. gpatrinos@upatras.gr.
Source: Human genomics [Hum Genomics] 2017 Dec 08; Vol. 11 (1), pp. 30. Date of Electronic Publication: 2017 Dec 08.
Publication Type: Journal Article
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101202210 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-7364 (Electronic) Linking ISSN: 14739542 NLM ISO Abbreviation: Hum Genomics Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1479-7364
DOI:10.1186/s40246-017-0126-2