- Title
- Familial Cortical Myoclonus with a Mutation in NOL3
- Creators
- Jonathan F RUSSELL - Department of Neurology, School of Medicine, University of California at San Francisco, San Francisco, CA, United StatesJamie L STECKLEY - Department of Clinical Neurological Sciences, London Health Sciences Center and University of Western Ontario, London, Ontario, CanadaMurim CHOI - Department of Genetics, Howard Hughes Medical Institute, School of Medicine, Yale University, New Haven, CT, United StatesHsien-Yang LEE - Department of Neurology, School of Medicine, University of California at San Francisco, San Francisco, CA, United StatesAndrew KIRK - Division of Neurology, Royal University Hospital, Saskatoon, Saskatchewan, CanadaCarol NELSON-WILLIAMS - Department of Genetics, Howard Hughes Medical Institute, School of Medicine, Yale University, New Haven, CT, United StatesGillian GIBSON - Neurology Division, University of British Columbia, Vancouver, British Columbia, CanadaScott C BARABAN - Epilepsy Research Laboratory, Department of Neurological Surgery, University of California at San Francisco, San Francisco, CA, United StatesRichard P LIFTON - Department of Genetics, Howard Hughes Medical Institute, School of Medicine, Yale University, New Haven, CT, United StatesDaniel H GESCHWIND - Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, United StatesYing-Hui FU - Department of Neurology, School of Medicine, University of California at San Francisco, San Francisco, CA, United StatesLouis J PTACEK - Department of Neurology, School of Medicine, University of California at San Francisco, San Francisco, CA, United StatesGiovanni COPPOLA - Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, United StatesAngelika F. G HAHN - Department of Clinical Neurological Sciences, London Health Sciences Center and University of Western Ontario, London, Ontario, CanadaMackenzie A HOWARD - Epilepsy Research Laboratory, Department of Neurological Surgery, University of California at San Francisco, San Francisco, CA, United StatesZachary KORNBERG - Department of Neurology, School of Medicine, University of California at San Francisco, San Francisco, CA, United StatesAlden HUANG - Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, United StatesSeyed M MIRSATTARI - Department of Clinical Neurological Sciences, London Health Sciences Center and University of Western Ontario, London, Ontario, CanadaBarry MERRIMAN - Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, United StatesEric KLEIN - Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, United States
- Publication Details
- Annals of neurology, Vol.72(2), pp.175-183
- Publisher
- Wiley-Liss
- Academic Unit
- Miller School of Medicine; UMMG Department of Ophthalmology
- Language
- English
- Resource Type
- Journal article
- PMID
- 22926851
- PMCID
- PMC3431191
- Record Identifier
- 991031598228002976
Journal article
Familial Cortical Myoclonus with a Mutation in NOL3
Annals of neurology, Vol.72(2), pp.175-183
2012
PMCID: PMC3431191
PMID: 22926851
Metrics
10 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.247 Migraines & Headaches
- 1.247.1001 Dystonia
- Web Of Science research areas
- Clinical Neurology
- Neurosciences
- ESI research areas
- Neuroscience & Behavior
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites