A Novel Mutation p.A59P in N-Terminal Domain of Methyl-CpG–Binding Protein 2 Confers Phenotypic Variability in 3 Cases of Tunisian Rett Patients

An AT-Hook Domain in MeCP2 Determines the Clinical Course of Rett Syndrome and Related Disorders

(2013) Steven Andrew Baker et al.   CELL

Spectrum of MECP2 gene mutations in a cohort of Indian patients with Rett syndrome: Report of two novel mutations

(2012) Dhanjit Kumar Das et al.   GENE

Investigating diproline segments in proteins: Occurrences, conformation and classification

(2011) Indranil Saha et al.   BIOPOLYMERS

Novel non-identical MECP2 mutations in Rett syndrome family: A rare presentation

(2011) Rajni Khajuria et al.   BRAIN & DEVELOPMENT

Trends in the Diagnosis of Rett Syndrome in Australia

(2011) Stephanie Fehr et al.   PEDIATRIC RESEARCH

Rett syndrome: Revised diagnostic criteria and nomenclature

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

A Novel MECP2 Gene Mutation in a Tunisian Patient with Rett Syndrome

(2009) Nourhène Fendri-Kriaa et al.   Genetic Testing and Molecular Biomarkers