Mutations of the same sequence of the myelin P0 gene causing two different phenotypes

Wiley, Human Mutation: Variation, Informatics and Disease, S1(11), p. S217-S219, 1998

Journal article published in 1998 by Federica Schiavon, Alessandra Rampazzo, Luciano Merlini

, Corrado Angelini, Maria L. Mostacciuolo

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