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

Journal of medical genetics

Volumn 37, Issue 12, 2000, Pages

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

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA BINDING PROTEIN; MECP2 PROTEIN, HUMAN; METHYL CPG BINDING PROTEIN 2; NONHISTONE PROTEIN; REPRESSOR PROTEIN;

AMINO ACID SEQUENCE; ASIAN; AUTISM; FEMALE; GENETICS; HUMAN; INFANT; LETTER; MISSENSE MUTATION; MOLECULAR GENETICS; NEWBORN; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; RETT SYNDROME; STOP CODON;

AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; AUTISTIC DISORDER; BASE SEQUENCE; CHILD, PRESCHOOL; CHROMOSOMAL PROTEINS, NON-HISTONE; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; METHYL-CPG-BINDING PROTEIN 2; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; REPRESSOR PROTEINS; RETT SYNDROME;

EID: 0034540747     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.37.12.e41     Document Type: Letter

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