- Title
- Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous : Families with and without MFN2 mutations
- Creators
- D ZHU - Neurobiology Laboratory, ANZAC Research Institute, University of Sydney, Concord Hospital, New South Wales, AustraliaM. L KENNERSON - Neurobiology Laboratory, ANZAC Research Institute, University of Sydney, Concord Hospital, New South Wales, AustraliaG WALIZADA - Neurobiology Laboratory, ANZAC Research Institute, University of Sydney, Concord Hospital, New South Wales, AustraliaS ZÜCHNER - Center for Human Genetics, Duke University Medical Center, Durham, NC, United StatesJ. M VANCE - Center for Human Genetics, Duke University Medical Center, Durham, NC, United StatesG. A NICHOLSON - Neurobiology Laboratory, ANZAC Research Institute, University of Sydney, Concord Hospital, New South Wales, Australia
- Publication Details
- Neurology, Vol.65(3), pp.496-497
- Publisher
- Lippincott Williams & Wilkins; Hagerstown, MD
- Academic Unit
- Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
- Language
- English
- Resource Type
- Journal article
- PMID
- 16087932
- Record Identifier
- 991031560835802976
Journal article
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous : Families with and without MFN2 mutations
Neurology, Vol.65(3), pp.496-497
2005
PMID: 16087932
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InCites Highlights
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- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.197 Molecular & Cell Biology - Mitochondria
- 1.197.564 Mitochondrial DNA
- Web Of Science research areas
- Clinical Neurology
- ESI research areas
- Neuroscience & Behavior
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Source: InCites