De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome

Author:

Sleven Hannah,Welsh Seth J.,Yu Jing,Churchill Mair E.A.,Wright Caroline F.,Henderson Alex,Horvath Rita,Rankin Julia,Vogt Julie,Magee Alex,McConnell Vivienne,Green Andrew,King Mary D.,Cox Helen,Armstrong Linlea,Lehman Anna,Nelson Tanya N.,Williams Jonathan,Clouston Penny,Hagman James,Németh Andrea H.

Funder

Action Medical Research

Henry Smith Charity

RP Fighting Blindness and Fight for Sight

Wendy Siegel Fund for Leukemia and Cancer Research

Victor W. Bolie and Earleen D. Bolie Graduate Scholarship Fund

Health Innovation Challenge Fund

Wellcome Trust Sanger Institute

Mining for Miracles

British Columbia Children’s Hospital Foundation

Genome British Columbia

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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