The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene
- 1 January 2003
- journal article
- research article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 13 (1) , 60-67
- https://doi.org/10.1016/s0960-8966(02)00196-7
Abstract
No abstract availableKeywords
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