Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation
Jiong Tao(University of Pittsburgh Medical Center), Vera M. Kalscheuer(Max Planck Institute for Molecular Genetics), Jozef Gécz(The University of Adelaide), M. Hagedorn-Greiwe, Martine Raynaud(Université de Tours), E. Schwinger, Hilde Van Esch, Jean‐Pierre Fryns, Kirsten Hoffmann(Max Planck Institute for Molecular Genetics), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), Jürgen Sperner(University of Lübeck), Bettina A. Moser(Max Planck Society)
Cited by 323
Related Papers
Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A
|Science|1993|1.6k
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
|The American Journal of Human Genetics|2004|760
Localization of the gene for Cowden disease to chromosome 10q22–23
|Nature Genetics|1996|670
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
|Nature Genetics|2009|617