Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy

Anna Lehman(University of British Columbia), Suzanne Vercauteren, Tara Candido(University of British Columbia), Christèle du Souich, Grazia M.S. Mancini(Erasmus MC), Linda Huh, Clara van Karnebeek, Ramona Salvarinova(University of British Columbia), Corneliu Bolbocean(University of British Columbia), Sonal Desai(Kennedy Krieger Institute), Ilaria Guella(University of British Columbia), Somayeh Mojard Kalkhoran(Simon Fraser University), Tamsin Tarling, Samrat Thouta(University of British Columbia), Graham Sinclair, Jill Mwenifumbo(University of British Columbia), Cyrus Boelman(University of British Columbia), Matthew J. Farrer(University of Florida), Michelle Demos(University of British Columbia), Mary Connolly, Jan M. Friedman(University of British Columbia Hospital), Shelin Adam(BC Children's Hospital), Daniel M. Evans, Marjon van Slegtenhorst(Erasmus MC), Marna B. McKenzie(University of British Columbia), Sarah E. Buerki, William T. Gibson(BC Children's Hospital), Katelin N. Townsend, Damon Poburko(Simon Fraser University), Tanya N. Nelson(University of British Columbia), Anita Datta(Northwestern University), Tom W. Claydon(Simon Fraser University), Kirsty McWalter, Gabriella Horváth(Children's & Women's Health Centre of British Columbia), Alison M. Elliott(Winnipeg Regional Health Authority), Sakkubai Naidu(Kennedy Krieger Institute), Richard Person(GenVec), Eric Toyota, Margot I. Van Allen, Patrice Eydoux(Hôpital Ambroise-Paré)
The American Journal of Human Genetics
June 29, 2017
Cited by 130


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