DOI:
10.1055/s-00000041
Neuropediatrics
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References
Hattori N, Yamamoto M, Yoshihara T. , et al; Study Group for Hereditary Neuropathy in Japan.
Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.
Brain 2003;
126 (Pt 1): 134-151
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