Keyphrases
Coding Sequence
100%
Autism
100%
Infantile Autism
100%
Methyl-CpG-binding Protein 2 (MeCP2)
100%
Mutation Analysis
100%
Coding Region
33%
Rett Syndrome
33%
Polymorphism
16%
Etiology
16%
Specific mutation
16%
Molecular Genetics
16%
Pedigree
16%
Ultra-high Performance Liquid Chromatography (UHPLC)
16%
Distinct Entity
16%
Sequence Variants
16%
Molecular Genetic Testing
16%
Intellectual Disability
16%
Rare Polymorphisms
16%
Silent mutation
16%
Functional Domain
16%
X-linked Mental Retardation
16%
Autism Syndrome
16%
Relative Pairs
16%
Direct Sequencing
16%
Neuroscience
Pervasive Developmental Disorder
100%
Methyl CpG Binding Protein 2
100%
Coding Region
50%
Rett Syndrome
50%
Mental Retardation Malformation Syndrome
25%
X Linked Mental Retardation
25%
Silent Mutation
25%
Biochemistry, Genetics and Molecular Biology
Binding Protein
100%
Molecular Genetics
50%
Rett Syndrome
50%
Coding Region
50%
Pedigree
25%
Silent Mutation
25%
High-Performance Liquid Chromatography
25%