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Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X
Kleopa, K. A., Zamba-Papanicolaou, E., Alevra, X., Nicolaou, P., Georgiou, D. -M., Hadjisavvas, A., Kyriakides, T., Christodoulou, K.Volume:
66
Language:
english
Journal:
Neurology
DOI:
10.1212/01.wnl.0000196479.93722.59
Date:
February, 2006
File:
PDF, 882 KB
english, 2006