Mutations in KPTN Cause Macrocephaly, Neurodevelopmental Delay, and Seizures

Emma L. Baple(University of Exeter), Andrew H. Crosby(University of Exeter), Tala Zainy(St George’s University Hospitals NHS Foundation Trust), Saeed Al-Turki(Wellcome Sanger Institute), Maryam Izadi(Jena University Hospital), Sahar Mansour(Princess Nourah bint Abdulrahman University), Michael M. Kessels(Jena University Hospital), Robert Pawlak(University of Exeter), Anna E. Skrzypiec(University of Exeter), Karin Wagner(Holmes Community College), Harold E. Cross(University of Arizona), Britta Qualmann(Jena University Hospital), Matt Hurles(Wellcome Sanger Institute), Barry A. Chioza(University of Exeter), Reza Maroofian(University College London), Katy Barwick(Great Ormond Street Hospital), Phillip Rich(St George's Hospital), Michael A. Patton(St George's Hospital), Roselyn Coblentz(Holmes Community College)
The American Journal of Human Genetics
November 14, 2013
Cited by 54


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