Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
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- 1 March 2002
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 70 (3), 726-736
- https://doi.org/10.1086/339274
Abstract
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