DOI:
10.1055/s-00034916
Nervenheilkunde
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References
De Sandre-Giovannoli A. et al
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.
American journal of human genetics 2002;
70 (03) 726-36.
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