Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2-Reference-Cited by-同舟云学术

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

Published:2006-01-25 Issue:2 Volume:59 Page:276-281
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Züchner Stephan¹,De Jonghe Peter²³,Jordanova Albena²⁴⁵,Claeys Kristl G.²³,Guergueltcheva Velina⁴,Cherninkova Sylvia⁴,Hamilton Steven R.⁶,Van Stavern Greg⁷,Krajewski Karen M.⁸,Stajich Jeffery¹,Tournev Ivajlo⁴,Verhoeven Kristien²,Langerhorst Christine T.⁹,de Visser Marianne¹⁰,Baas Frank¹⁰¹¹,Bird Thomas¹²,Timmerman Vincent²,Shy Michael⁸,Vance Jeffery M.¹

Affiliation:

1. Center for Human Genetics, and Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC

2. Molecular Genetics Department, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Belgium

3. Division of Neurology, University Hospital Antwerp, Antwerp, Belgium

4. Department of Neurology, Sofia Medical University, Sofia, Bulgaria

5. Laboratory of Molecular Pathology, Sofia Medical University, Sofia, Bulgaria

6. Neuro‐ophthalmology Unit, Neuroscience Institute, Swedish Medical Center, Seattle, WA

7. Kresge Eye Institute, Wayne State University School of Medicine, Detroit, MI

8. Department of Neurology, Wayne State University School of Medicine, Detroit, MI

9. Department of Ophthalmology, Academic Medical Center, Amsterdam, the Netherlands

10. Department of Neurology, Academic Medical Center, Amsterdam, the Netherlands

11. Neurogenetics Laboratory, Academic Medical Center, Amsterdam, the Netherlands

12. Department of Neurology, University of Washington, Geriatric Research Center, VA Medical Center, Seattle, WA

Funder

CMT families

NIH

NINDS grants

Fund for Scientific Research-Flanders

Medical Foundation Queen Elisabeth

University of Antwerp

Interuniversity Attraction Poles program of the Belgian Federal Science Office

Netherlands Organization for Health Research and Development

VA Research Funds

Visiting research fellowships from the POD

NATO/FWO. a postdoctoral fellow of the FWO, Belgium

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.20797

Reference24 articles.

1. Genetic and clinical aspects of Charcot-Marie-Tooth's disease

2. Hereditary Motor and Sensory Neuropathies: An Overview of Clinical, Genetic, Electrophysiologic, and Pathologic Features

3. Peripheral neuropathy;Dyck PJ,1993

4. Hereditary Motor and Sensory Neuropathy With Optic Atrophy

5. Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.

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