WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome

Cori De Santo, Kristin D'Aco, Gabriel C. Araujo, Nora Shannon, D. D.D. Study, Hilary Vernon, April Rahrig, Kristin G. Monaghan, Zhiyv Niu, Patrik Vitazka, Jonathan Dodd, Sha Tang, Linda Manwaring, Arelis Martir-Negron, Rhonda E. Schnur, Jane Juusola, Audrey Schroeder, Vivian Pan, Katherine L. Helbig, Bethany FriedmanMarwan Shinawi

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences