A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development - Elisa De Franco, Chi C. Wong, Watson Ra, Rachel A. Watson, Wolfgang J. Weninger, Weninger Wj, Flanagan Se, Angela Green, Caswell R., Catherine Tudor, Christopher J. Lelliott, Barbara Maurer-Gesek, Lukas F. Reissig, De Franco E., Geyer Sh - Dissemin

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Yearbook of Paediatric Endocrinology, 2019

DOI: 10.1530/ey.16.2.7

Cell Press, American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2019.03.018

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A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development

Journal article published in 2019 by Elisa De Franco, Chi C. Wong, Watson Ra, Rachel A. Watson, Wolfgang J. Weninger, Weninger Wj, Flanagan Se, Angela Green, Caswell R., Catherine Tudor, Christopher J. Lelliott, Barbara Maurer-Gesek, Lukas F. Reissig, De Franco E., Geyer Sh and other authors.

This paper is made freely available by the publisher.

This paper is made freely available by the publisher.

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