DOI:
10.1055/s-00000004
Aktuelle Neurologie
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References
De Sandre-Giovannoli A, Chaouch M, Kozlov S 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.
Am J Hum Genet 2002;
70: 726-736
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