Inherited Peripheral Neuropathies Mutation Database

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Reference

Title The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.
Authors De Jonghe P, Timmerman V, Ceuterick C, Nelis E, De Vriendt E, Löfgren A, Vercruyssen A, Verellen C, Van Maldergem L, Martin JJ, Van Broeckhoven C
Reference Brain 122: 281-290, 1999 (PubMed ID: 10071056 )
MPZ (P0): (Thr124Met)
Mutations

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