A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development
Titel:
A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development
Auteur:
De Franco, Elisa Watson, Rachel A. Weninger, Wolfgang J. Wong, Chi C. Flanagan, Sarah E. Caswell, Richard Green, Angela Tudor, Catherine Lelliott, Christopher J. Geyer, Stefan H. Maurer-Gesek, Barbara Reissig, Lukas F. Lango Allen, Hana Caliebe, Almuth Siebert, Reiner Holterhus, Paul Martin Deeb, Asma Prin, Fabrice Hilbrands, Robert Heimberg, Harry Ellard, Sian Hattersley, Andrew T. Barroso, InĂªs