Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Reham Alharatani(King's College London), Karen Liu(Wilfrid Laurier University), Ana Beleza‐Meireles(King's College London), Elaine H. Zackai(Children's Hospital of Philadelphia), Alex Cash(Guy's and St Thomas' NHS Foundation Trust), Ping Yee Billie Au(University of Calgary), Richard H. Scott(Genomics England), Natsuko Neo(Tokyo Medical and Dental University), Diana Baralle(Princess Anne Hospital), John N. Griffin(Yale University), Emily K. Mis(Yale University), Nabina Bhujel(Guy's and St Thomas' NHS Foundation Trust), Denise K. Marciano(The University of Texas Southwestern Medical Center), Caitlin A. Chang(University of Calgary), Marie Thérèse Hosey(King's College London), Mustafa K. Khokha(Yale University), Quinten Patterson(The University of Texas Southwestern Medical Center), Christopher Healy(King's College London), Meriel McEntagart(St George's, University of London), Weizhen Ji(Howard Hughes Medical Institute), Ruth Newbury‐Ecob(University Hospitals Bristol NHS Foundation Trust), Ruth Cleaver(Royal Devon and Exeter Hospital), Monica Konstantino(Yale University), Saquib A. Lakhani(Yale University), Sumayyah Hannan(King's College London), Elizabeth Bhoj(Children's Hospital of Philadelphia), Dong Li(Children's Hospital of Philadelphia), Abhijit Dixit(Nottingham City Hospital), Jane A. Hurst(Great Ormond Street Hospital), Athina Ververi(Great Ormond Street Hospital for Children NHS Foundation Trust)

Human Molecular Genetics

March 17, 2020

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