|ITEM METADATA RECORD
|Title: ||Mutations in Mitofusin 2 are a major cause for autosomal dominant axonal CMT neuropathy|
|Authors: ||Claeys, Kristl|
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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