A Rare Homozygous Missense Mutation in ATP7B Exon 19 in a Case of Wilson Disease

Publisher: Karger

E-ISSN: 1421-9913|51|1|52-54

ISSN: 0014-3022

Source: European Neurology, Vol.51, Iss.1, 2004-01, pp. : 52-54

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