University of Münster
CRIS@UM
DE | EN

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.

Diener S, Bayer S, Sabrautzki S, Wieland T, Mentrup B, Przemeck GK, Rathkolb B, Graf E, Hans W, Fuchs H, Horsch M, Schwarzmayr T, Wolf E, Klopocki E, Jakob F, Strom TM, Hrabě de Angelis M, Lorenz-Depiereux B

Research article (journal) | Peer reviewed

Details about the publication

Volume: 27
Issue: 3-4
Page range: 111-121
Status: Published
Release year: 2016
Language in which the publication is written: English
DOI: 10.1007/s00335-016-9619-x.

Authors from the University of Münster

Mentrup, Birgit
Institute of Musculoskeletal Medicine (IMM)