Adolescent onset cognitive regression and neuropsychiatric symptoms associated with the A140V MECP2 mutation

Altered Attainment of Developmental Milestones Influences the Age of Diagnosis of Rett Syndrome

(2011) Stephanie Fehr et al.   JOURNAL OF CHILD NEUROLOGY

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutation

(2011) Eri Takeshita et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Rett syndrome: Revised diagnostic criteria and nomenclature

(2010) Jeffrey L. Neul et al.   ANNALS OF NEUROLOGY

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

(2010) Garilyn M Jentarra et al.   BMC NEUROSCIENCE

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

(2009) R. C. Samaco et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

(2008) J. L. Neul et al.   NEUROLOGY

Investigating genotype-phenotype relationships in Rett syndrome using an international data set

(2008) A. Bebbington et al.   NEUROLOGY