Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.
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E. Mariman | F. Gabreëls | P. Jongen | B. V. van Engelen | L. Valentijn | S. V. van Beersum | P. Bolhuis | A. Gabreëls-Festen | P. Lenssen | P. J. van Wensen