Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

J Med Genet. 2000 Dec;37(12):E41. doi: 10.1136/jmg.37.12.e41.

Authors

C W Lam, W L Yeung, C H Ko, P M Poon, S F Tong, K Y Chan, I F Lo, L Y Chan, J Hui, V Wong, C P Pang, Y M Lo, T F Fok

No abstract available

Publication types

Letter

MeSH terms

Amino Acid Sequence
Asian People / genetics
Autistic Disorder / genetics*
Base Sequence
Child, Preschool
Chromosomal Proteins, Non-Histone*
Codon, Nonsense*
DNA Mutational Analysis
DNA-Binding Proteins / genetics*
Female
Humans
Infant
Infant, Newborn
Methyl-CpG-Binding Protein 2
Molecular Sequence Data
Mutation, Missense*
Repressor Proteins / genetics*
Rett Syndrome / genetics*

Substances

Chromosomal Proteins, Non-Histone
Codon, Nonsense
DNA-Binding Proteins
MECP2 protein, human
Methyl-CpG-Binding Protein 2
Repressor Proteins