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Paper Details

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
Am J Hum Genet
111
2017
CAMK2, CAMK2A, CAMK2B, CAMK2B variants, Calcium, Calcium/calmodulin-dependent protein kinase II, Intellectual Disability, Protein Kinase Genes, Thr286, Thr287, human, intellectual disability, mice, neuronal
Author NameAffiliation
Megan T Cho
Stephan J SandersUCSF Weill Institute for Neurosciences, University of California san francisco
Jonathan A BernsteinStanford University School of Medicine
Wilfrid CarréCHU de Rennes
Tabib DabirBelfast City Hospital
Ghayda M MirzaaUniversity of Washington School of Medicine and Seattle Children's Hospital, USA Center for Integrative Brain Research, Seattle Children's Research Institute
Gregory M EnnsStanford University School of Medicine
Nagarajan ParamasivamHeidelberg University, German Cancer Research Center (DKFZ)
Catherine A BrownsteinBoston Children's Hospital and Harvard Medical School, The Manton Center for Orphan Disease Research
Catherine A BrownsteinBoston Children's Hospital and Harvard Medical School, The Manton Center for Orphan Disease Research
Vernon R Sutton
Jay ShendureUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute
Jay ShendureUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute
Yaping YangBaylor College of Medicine
Matthew W StateUCSF Weill Institute for Neurosciences, University of California san francisco
Matthew W StateUCSF Weill Institute for Neurosciences, University of California san francisco
Evan E EichlerUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute
Evan E EichlerUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute
Pankaj B AgrawalBoston Children's Hospital and Harvard Medical School, The Manton Center for Orphan Disease Research
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