High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation
Efraim H. Rosenberg(University Medical Center), Gajja S. Salomons(Amsterdam Neuroscience), Lígia S. Almeida(University Medical Center), Helger G. Yntema(Radboud University Nijmegen), Rose S. deGrauw(University Medical Center), Tjitske Kleefstra(Radboud University Nijmegen), Claude Moraine(Inserm), Jean‐Pierre Fryns, Nadia Bahi(Inserm), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), Cornelis Jakobs(University Medical Center), Ton J. deGrauw(Cincinnati Children's Hospital Medical Center)
Cited by 213
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