Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2

J. Colomer, R.L. Gooding, Dora Angelicheva, R.H.M. King, E. Guillen-Navarro, Y. Parman, A. Nascimento, J. Conill, Luba Kalaydjieva

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