The Thr124Met mutation in the peripheral myelin protein zero ( MPZ ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype

Author： De Jonghe P   Timmerman V   Ceuterick C   Nelis E   De Vriendt E   Löfgren A   Vercruyssen A   Verellen C   Van Maldergem L   Martin J-J   Van Broeckhoven C  

Publisher： Oxford University Press

ISSN： 1460-2156

Source： Brain, Vol.122, Iss.2, 1999-02, pp. : 281-290

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