Is Rett syndrome a loss-of-imprinting disorder?

Nature Genetics

Volumn 37, Issue 1, 2005, Pages 10-11

  Pescucci, Chiara ^a   Meloni, Ilaria ^a   Renieri, Alessandra ^a  

^a UNIVERSITY OF SIENA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; BRAIN DERIVED NEUROTROPHIC FACTOR; DNA; HISTONE DEACETYLASE;

ANIMAL MODEL; CHROMATIN STRUCTURE; CPG ISLAND; DEVELOPMENTAL DISORDER; DLX5 GENE; DLX6 GENE; DNA SEQUENCE; GENE; GENE LOCUS; GENE MUTATION; GENETIC TRANSCRIPTION; MECP2 GENE; MOUSE; NERVE CELL; NEUROLOGIC DISEASE; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; RETT SYNDROME; SHORT SURVEY;

ANIMALS; CHROMATIN; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA-BINDING PROTEINS; GAMMA-AMINOBUTYRIC ACID; GENE EXPRESSION PROFILING; GENOMIC IMPRINTING; HOMEODOMAIN PROTEINS; HUMANS; METHYL-CPG-BINDING PROTEIN 2; MICE; NEURONS; REPRESSOR PROTEINS; RETT SYNDROME; TRANSCRIPTION FACTORS;

ANIMALIA;

EID: 11244263191     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0105-10     Document Type: Short Survey

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