Assignment of an ionotropic glutamate receptor-like gene (GRINL1A) to human chromosome 15q22.1 by in situ hybridization

Cytogenetics and Cell Genetics

Volumn 93, Issue 1-2, 2001, Pages 143-144

  Roginski, Raymond S ^a   Mohan Raj, B K ^a   Finkernagel, S W ^a   Sciorra, L J ^a  

^a ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IONOTROPIC RECEPTOR;

ANIMAL CELL; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 15Q; DNA LIBRARY; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCATION; GENE MAPPING; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RAT;

AUTISTIC DISORDER; CHROMOSOMES, HUMAN, PAIR 15; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PHYSICAL CHROMOSOME MAPPING; RECEPTORS, GLUTAMATE;

EID: 0034904457     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (4)

1. Hypothesis: Is infantile autism a hypoglutamatergic disorder? Relevance of glutamate-serotonin interactions for pharmacotherapy
2. Increased NMDA current and spine density in mice lacking the NMDA receptor subunit NR3A
3. Analysis of a 1-megabase deletion in 15q22→q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22→q23 and 15q11→q13
4. Chromosome mapping of three human LAMMER protein-kinase encoding genes