GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome
Dan Doherty(University of Washington), Teresa Zelinski(Research Manitoba), Gail Coghlan(Children's Hospital Research Institute of Manitoba), Albert E. Chudley(University of Manitoba), Ian G. Phelps(University of Washington), A. Micheil Innes(University of Calgary), Moien Kanaan(Diyarbakır Askeri Hastanesi), Mustafa Tekin(University of Miami), Hashem Shahin(Bethlehem University), Anthony P. Fejes(Canada's Michael Smith Genome Sciences Centre), Hatice Akay(Diyarbakır Askeri Hastanesi), Steven J.M. Jones(University of British Columbia), R. Curtis Rogers(Greenwood Genetic Center), Edmond G. Lemire(University of Saskatchewan), Gisele E. Ishak(Seattle Children's Hospital), Aizeddin A. Mhanni(University of Manitoba), Barbara L. Triggs‐Raine(Children's Hospital Research Institute of Manitoba), Shing H. Zhan(Canada's Michael Smith Genome Sciences Centre)
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