Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation

Author： Lenssen PPA   Gabreëls-Festen AAWM   Valentijn LJ   Jongen PJH   van Beersum SEC   van Engelen BGM   van Wensen PJM   Bolhuis PA   Gabreëls FJM   Mariman ECM  

Publisher： Oxford University Press

ISSN： 1460-2156

Source： Brain, Vol.121, Iss.8, 1998-08, pp. : 1451-1458

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