- Title
- Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia
- Creators
- Magdalena ZIMON - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumJonathan BAETS - Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumMichaela AUER-GRUMBACH - Department of Internal Medicine, Division of Endocrinology and Metabolism, Medical University of Graz, Graz, AustriaPeter DE RIJK - Applied Molecular Genomics Unit, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumBritt-Sabina PETERSEN - Institute of Clinical Molecular Biology, Christian-Albrechts-University, Kiel, GermanyThomas MÜLLER - Department of Pediatrics II, Innsbruck Medical University, Innsbruck, AustriaErik FRANSEN - Department of Medical Genetics, University of Antwerp, Antwerp, BelgiumPhilip VAN DAMME - Experimental Neurology, University of Leuven, Leuven, BelgiumWolfgang N LÖSCHER - Department of Neurology, Innsbruck Medical University, Innsbruck, AustriaNina BARISIC - Department of Paediatrics, University of Zagreb, Medical School, University Hospital Centre Zagreb, Zagreb, CroatiaZoran MITROVIC - National Center for Neuromuscular Diseases, Department of Neurology, University Hospital Center Zagreb, Zagreb, CroatiaStefanoc PREVITALI - Division of Neuroscience, Institute for Experimental Neurology, San Raffaele Scientific Institute, Milan, ItalyLeonardo ALMEIDA-SOUZA - Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumHaluk TOPALOGLU - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumGünther BERNERT - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumAna BELEZA-MEIRELES - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumSlobodanka TODOROVIC - Clinic for Neurology and Psychiatry for Children and Youth, University of Belgrade, Belgrade, SerbiaDusanka SAVIC-PAVICEVIC - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumBoryana ISHPEKOVA - Department of Cognitive Science and Psychology, New Bulgarian University, Sofia, BulgariaSilvia LECHNER - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumKristien PEETERS - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumTinne OOMS - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumAngelika F HAHN - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumEls DE VRIENDT - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumStephan ZÜCHNER - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumVincent TIMMERMAN - Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumPatrick VAN DIJCK - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumVedrana Milic RASIC - Clinic for Neurology and Psychiatry for Children and Youth, University of Belgrade, Belgrade, SerbiaAndreasr JANECKE - Department of Pediatrics II, Innsbruck Medical University, Innsbruck, AustriaPeter DE JONGHE - Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumAlbena JORDANOVA - Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp, BelgiumJelena NIKODINOVIC - Clinic for Neurology and Psychiatry for Children and Youth, University of Belgrade, Belgrade, SerbiaYesim PARMAN - Department of Neurology, Istanbul Medical Faculty, Istanbul University, Istanbul, TurkeyEsra BATTALOGLU - Department of Molecular Biology and Genetics, Bogazici University, Istanbul, TurkeyZeliha MATUR - Department of Neurology, Istanbul Medical Faculty, Istanbul University, Istanbul, TurkeyVelina GUERGUELTCHEVA - Department of Neurology, Medical University-Sofia, Sofia, BulgariaIvailo TOURNEV - Department of Cognitive Science and Psychology, New Bulgarian University, Sofia, Bulgaria
- Publication Details
- Nature genetics, Vol.44(10), pp.1080-1083
- Publisher
- Nature Publishing Group; New York, NY
- Academic Unit
- Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics
- Language
- English
- Resource Type
- Journal article
- PMID
- 22961002
- Record Identifier
- 991031559804802976
Journal article
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia
Nature genetics, Vol.44(10), pp.1080-1083
2012
PMID: 22961002
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- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.253 Nerve Disorders
- 1.253.1972 Charcot-Marie-Tooth Disease
- Web Of Science research areas
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
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Source: InCites