Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position
作者单位：Ruhr-University, MA 5/39, 44780 Bochum, Germany[1]Servicio de Neurología, Hospital del Ni?o Jesús, Tucumán, Argentina[2]Departamento Biomédico, Facultad de Medicina, Universidad Nacional de Tucuman, Argentina[3]Laboratorio di Genetica Umana, Dipartimento di Biologia, Università di Padova, Padova, Italy[4]Department of Neurosciences, Psychiatry and Anaesthesiology, AOU G. Martino, University of Messina[5]
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