Disturbed copper transport in humans. Part 2: Mutations of the ATP7B gene lead to Wilson Disease (WD)

J. Seidel, K. Caca, Sibylle Schwab, F. Berr, Dieter Wildenauer, H.J. Mentzel, N. Horn, E. Kauf

    Research output: Contribution to journalArticlepeer-review

    5 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)OL149-OL157
    JournalCellular and Molecular Biology
    Issue number21
    Publication statusPublished - 2001

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