Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome
M. Chiara Manzini(Rutgers, The State University of New Jersey), Christopher A. Walsh(Boston Children's Hospital), Vandana Gupta(Brigham and Women's Hospital), Mustafa A. Salih(King Saud University), Jacqueline Rodriguez(Boston Children's Hospital), Christine Stevens(Broad Institute), Kevin V. Shianna(Duke University), Erin L. Heinzen(University of North Carolina at Chapel Hill), Jennifer N. Partlow(Broad Institute), Robin D. Clark(Loma Linda University Children's Hospital), Abdelkarim A. Al-Qudah(University of Jordan), Jan M. Friedman(University of British Columbia Hospital), Alan H. Beggs(Boston Children's Hospital), Wafaa Eyaid(King Saud bin Abdulaziz University for Health Sciences), Stacey Gabriel(Broad Institute), Timothy W. Yu(Boston Children's Hospital), Brenda J. Barry(Boston Children's Hospital), Thomas M. Maynard(Carilion Clinic), Isabella Moroni(Vita-Salute San Raffaele University), Marina Mora(Fondazione IRCCS Istituto Neurologico Carlo Besta), Dimira Tambunan(Boston Children's Hospital), R. Sean Hill(Boston Children's Hospital)
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