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Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease

J Genschel1, A Czlonkowska, G Sommer

  • 1Campus Charité Mitte, Med. Klinik m.S. Gastroenterologie, Hepatologie und Endokrinologie, Berlin, Germany.

Human Mutation
|February 17, 2001
PubMed
Summary

No abstract available in PubMed .

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