G.O. 9 Dynamin 2 mutations are associated with dominant intermediate Charcot-Marie-Tooth disease and dominant centronuclear myopathy

K.G Claeys; S Züchner; M Kennerson; K Verhoeven; C Ceuterick; J.J Martin; J Berciano; J.M Vance; G Nicholson; V Timmerman; P De Jonghe

doi:10.1016/j.nmd.2006.05.256

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G.O. 9 Dynamin 2 mutations are associated with dominant intermediate Charcot-Marie-Tooth disease and dominant centronuclear myopathy

Journal article

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G.O. 9 Dynamin 2 mutations are associated with dominant intermediate Charcot-Marie-Tooth disease and dominant centronuclear myopathy

K.G Claeys, S Züchner, M Kennerson, K Verhoeven, C Ceuterick, J.J Martin, J Berciano, J.M Vance, G Nicholson, V Timmerman, …

Neuromuscular disorders : NMD, Vol.16(9), pp.725-725

2006

DOI: https://doi.org/10.1016/j.nmd.2006.05.256

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Title: G.O. 9 Dynamin 2 mutations are associated with dominant intermediate Charcot-Marie-Tooth disease and dominant centronuclear myopathy
Creators: K.G Claeys - Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerp, Belgium
S Züchner - Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, USA
M Kennerson - Northcott Neuroscience Laboratory, ANZAC Research Institute, New South Wales, Australia
K Verhoeven - Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerp, Belgium
C Ceuterick - Department of Neuropathology, Institute Born Bunge, University of Antwerp, Antwerp, Belgium
J.J Martin - Department of Neurology, University Hospital Antwerp, Antwerp, Belgium
J Berciano - Service of Neurology, University Hospital “Marqués de Valdecilla”, Santander, Spain
J.M Vance - Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, USA
G Nicholson - Northcott Neuroscience Laboratory, ANZAC Research Institute, New South Wales, Australia
V Timmerman - Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerp, Belgium
P De Jonghe - Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerp, Belgium
Publication Details: Neuromuscular disorders : NMD, Vol.16(9), pp.725-725
Publisher: Elsevier B.V
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
Record Identifier: 991031600359402976