1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay

American Journal of Medical Genetics, Part A

Volumn 164, Issue 2, 2014, Pages 456-460

  Takenouchi, Toshiki ^a   Hashida, Noriko ^a   Torii, Chiharu ^a   Kosaki, Rika ^b   Takahashi, Takao ^a   Kosaki, Kenjiro ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NATIONAL CENTER FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

Author keywords

Developmental delay; Glutamate receptor; GRIK3

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 1P; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISORDER; FAILURE TO THRIVE; FEMALE; GENE; GRIK3 GENE; HUMAN; LANGUAGE DEVELOPMENT; MICROARRAY KIT; MOTIVATION; MOTOR DEVELOPMENT; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PSYCHOSOCIAL DEVELOPMENT; WEIGHT GAIN;

DEVELOPMENTAL DELAY; GLUTAMATE RECEPTOR; GRIK3;

ADULT; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; FACIES; FEMALE; HUMANS; MALE; PHENOTYPE; RECEPTORS, KAINIC ACID;

EID: 84892838679     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36240     Document Type: Article

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