. . . . . "LMNA" . . . . "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" . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .