ArticleAmerican journal of human genetics2002
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.
Annachiara De Sandre-Giovannoli et al.PubMed ↗Full text ↗Publisher ↗
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