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 journalArticle

    4 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)OL149-OL157
    JournalCellular and Molecular Biology
    Volume47
    Issue number21
    Publication statusPublished - 2001

    Cite this

    Seidel, J., Caca, K., Schwab, S., Berr, F., Wildenauer, D., Mentzel, H. J., ... Kauf, E. (2001). Disturbed copper transport in humans. Part 2: Mutations of the ATP7B gene lead to Wilson Disease (WD). Cellular and Molecular Biology, 47(21), OL149-OL157.