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Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease

D Pareyson1, D Menichella, S Botti

  • 1Istituto Nazionale Neurologico C. Besta, Milan, Italy. dpareys@tin.it

Annals of the New York Academy of Sciences
|December 10, 1999
PubMed
Abstract

No abstract available in PubMed .

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