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Allele Publication :

Type  Used-FC Publication . Mgi Jnum  J:75378
Publication . Citation  De Sandre-Giovannoli A, et al. (2002) 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. Am J Hum Genet 70(3):726-36
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