Journal article

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis

Hilary C Martin, Grace E Kim, Alistair T Pagnamenta, Yoshiko Murakami, Gemma L Carvill, Esther Meyer, Richard R Copley, Andrew Rimmer, Giulia Barcia, Matthew R Fleming, Jack Kronengold, Maile R Brown, Karl A Hudspith, John Broxholme, Alexander Kanapin, Jean-Baptiste Cazier, Taroh Kinoshita, Rima Nabbout, David Bentley, Gil McVean Show all

HUMAN MOLECULAR GENETICS | OXFORD UNIV PRESS | Published : 2014

University of Melbourne Researchers

Grants

Awarded by Wellcome Trust


Awarded by NIH


Awarded by Medical Research Council


Awarded by EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT


Awarded by EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT


Funding Acknowledgements

This work was supported in part by a Wellcome Trust Core Award (090532/Z/09/Z) to the Wellcome Trust Centre for Human Genetics and a Wellcome Trust Senior Investigator Award to P. D. (095552/2/11/2), in part by NIH grant HD067517 and in part by the Oxford NIHR Biomedical Research Centre. Funding to pay the Open Access publication charges for this article was provided by the wellcome Trust and the Oxford NIHR Biomedical Research Centre.