Title: Mutations in Mitofusin 2 are a major cause for autosomal dominant axonal CMT neuropathy
Authors: Claeys, Kristl
Verhoeven, K
Züchner, S
Schröder, JM
Vance, JM
Timmerman, V
De Jonghe, P
Issue Date: 2005
Conference: International Symposium on Neuromuscular Diseases location:Brussels, Belgium date:14-15 October 2005
Publication status: published
KU Leuven publication type: IMa
Appears in Collections:Laboratory for Muscle Diseases and Neuropathies

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