Showing 1 - 1 results of 1 for search 'Kathrin Kühni Boghenbor', query time: 0.02s Refine Results
  1. 1
    An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle.

    An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. by Cord Drögemüller, Ursula Reichart, Torsten Seuberlich, Anna Oevermann, Martin Baumgartner, Kathrin Kühni Boghenbor, Michael H Stoffel, Claudia Syring, Mireille Meylan, Simone Müller, Mathias Müller, Birgit Gredler, Johann Sölkner, Tosso Leeb

    Published 2011-04-01
    Get full text
    Article

Search Tools: