MECP2 mutation in a boy with language disorder and schizophrenia.

The American journal of psychiatry

Volumn 159, Issue 1, 2002, Pages 148-149

  Cohen, David ^a   Lazar, Gabriela ^a   Couvert, Philippe ^a   Desportes, Vincent ^a   Lippe, Didier ^a   Mazet, Philippe ^a   Héron, Delphine ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

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

ADOLESCENT; AMINO ACID SUBSTITUTION; CASE REPORT; CHILD; FOLLOW UP; GENETICS; HUMAN; LANGUAGE DISABILITY; LETTER; MALE; MISSENSE MUTATION; PSYCHOLOGICAL ASPECT; SCHIZOPHRENIA;

ADOLESCENT; ALANINE; AMINO ACID SUBSTITUTION; CHILD; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA-BINDING PROTEINS; FOLLOW-UP STUDIES; HUMANS; LANGUAGE DEVELOPMENT DISORDERS; MALE; METHYL-CPG-BINDING PROTEIN 2; MUTATION, MISSENSE; REPRESSOR PROTEINS; SCHIZOPHRENIA, CHILDHOOD; VALINE;

MLCS; MLOWN;

EID: 0036371289     PISSN: 0002953X     EISSN: None     Source Type: Journal    
DOI: 10.1176/appi.ajp.159.1.148-a     Document Type: Letter

References (0)