HTR2A variation and sudden infant death syndrome: A case-control analysis

Acta Paediatrica, International Journal of Paediatrics

Volumn 98, Issue 1, 2009, Pages 58-61

  Rand, Casey M ^a   Berry Kravis, Elizabeth M ^a,b   Fan, Wenqing ^b   Weese Mayer, Debra E ^c,d  

^a Rush Children's Hospital and Rush University Medical Center   (United States)

^b RUSH UNIVERSITY MEDICAL CENTER   (United States)

^c NORTHWESTERN UNIVERSITY   (United States)

^d CHILDREN'S MEMORIAL HOSPITAL   (United States)

Author keywords

Autonomic nervous system; HTR2A; Serotonin; Serotonin receptor gene 2A; Sudden infant death syndrome

Indexed keywords

SEROTONIN 2A RECEPTOR;

ARTICLE; EXON; GENE AMPLIFICATION; GENE FREQUENCY; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HOMEOSTASIS; HUMAN; HYPOXIA; INTRON; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; RESPIRATORY FUNCTION; RISK ASSESSMENT; SEROTONINERGIC SYSTEM; SUDDEN INFANT DEATH SYNDROME;

ANOXIA; AUTONOMIC NERVOUS SYSTEM; CASE-CONTROL STUDIES; FEMALE; GENETIC VARIATION; HUMANS; INFANT; MALE; POLYMORPHISM, GENETIC; RECEPTOR, SEROTONIN, 5-HT2A; RISK FACTORS; SEROTONIN; SUDDEN INFANT DEATH;

EID: 57449102352     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2008.01018.x     Document Type: Article

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