Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation
Kerstin Kutsche(Universität Hamburg), Andreas Gal(Universität Hamburg), Maria Guida Boavida(Centro de Genética Clínica), Hans van Bokhoven(Radboud University Nijmegen), D. David(Centro de Genética Clínica), Ulrike Orth(Universität Hamburg), I. Jantke(Universität Hamburg), Helger G. Yntema(Radboud University Nijmegen), Ben C.J. Hamel(Radboud University Nijmegen), Hans Gerd Nothwang(Max Planck Institute for Molecular Genetics), Claude Moraine(Inserm), Jean‐Pierre Fryns, Alexander Brandt(Universität Hamburg), Jamel Chelly(Harvard University Press), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics)
Cited by 374
Related Papers
Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A
|Science|1993|1.6k
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
|PubMed|1989|961
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