Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Stephan ZÜCHNER; Peter DE JONGHE; Ivajlo TOURNEV; Kristien VERHOEVEN; Christine T LANGERHORST; Marianne DE VISSER; Frank BAAS; Thomas BIRD; Vincent TIMMERMAN; Michael SHY; Jeffery M VANCE; Albena JORDANOVA; Kristl G CLAEYS; Velina GUERGUELTCHEVA; Sylvia CHERNINKOVA; Steven R HAMILTON; Greg VAN STAVERN; Karen M KRAJEWSKI; Jeffery STAJICH

doi:10.1002/ana.20797

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Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Journal article

Peer reviewed

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Stephan ZÜCHNER, Peter DE JONGHE, Ivajlo TOURNEV, Kristien VERHOEVEN, Christine T LANGERHORST, Marianne DE VISSER, Frank BAAS, Thomas BIRD, Vincent TIMMERMAN, Michael SHY, …

Annals of neurology, Vol.59(2), pp.276-281

2006

DOI: https://doi.org/10.1002/ana.20797

PMID: 16437557

Abstract

Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction

Neurology

Biological and medical sciences

Medical sciences

Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases

Nervous system (semeiology, syndromes)

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275 Times Cited - Web of Science

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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; Neurosciences
ESI research areas: Neuroscience & Behavior

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Details

Title: Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
Creators: Stephan ZÜCHNER - Center for Human Genetics, and Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, United States
Peter DE JONGHE - Molecular Genetics Department, Flanders Interuniversiry Institute for Biotechnology, University of Antwerp, Belgium
Ivajlo TOURNEV - Department of Neurology, Sofia Medical University, Sofia, Bulgaria
Kristien VERHOEVEN - Molecular Genetics Department, Flanders Interuniversiry Institute for Biotechnology, University of Antwerp, Belgium
Christine T LANGERHORST - Department of Ophthalmology, Academic Medical Center, Amsterdam, Netherlands
Marianne DE VISSER - Department of Neurology, Academic Medical Center, Amsterdam, Netherlands
Frank BAAS - Department of Neurology, Academic Medical Center, Amsterdam, Netherlands
Thomas BIRD - Department of Neurology, University of Washington, Geriatric Research Center, VA Medical Center, Seattle, WA, United States
Vincent TIMMERMAN - Molecular Genetics Department, Flanders Interuniversiry Institute for Biotechnology, University of Antwerp, Belgium
Michael SHY - Department of Neurology, Wayne State University School of Medicine, Detroit, MI, United States
Jeffery M VANCE - Center for Human Genetics, and Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, United States
Albena JORDANOVA - Molecular Genetics Department, Flanders Interuniversiry Institute for Biotechnology, University of Antwerp, Belgium
Kristl G CLAEYS - Molecular Genetics Department, Flanders Interuniversiry Institute for Biotechnology, University of Antwerp, Belgium
Velina GUERGUELTCHEVA - Department of Neurology, Sofia Medical University, Sofia, Bulgaria
Sylvia CHERNINKOVA - Department of Neurology, Sofia Medical University, Sofia, Bulgaria
Steven R HAMILTON - Neuroophthalmology Unit, Neuroscience Institute, Swedish Medical Center, Seattle, WA, United States
Greg VAN STAVERN - Kresge Eye Institute, Wayne State University School of Medicine, Detroit, MI, United States
Karen M KRAJEWSKI - Department of Neurology, Wayne State University School of Medicine, Detroit, MI, United States
Jeffery STAJICH - Center for Human Genetics, and Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, United States
Publication Details: Annals of neurology, Vol.59(2), pp.276-281
Publisher: Willey-Liss; Hoboken
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: 16437557
Record Identifier: 991031560740602976