Sudden infant death syndrome: Rare mutation in the serotonin system FEV gene

Pediatric Research

Volumn 62, Issue 2, 2007, Pages 180-182

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

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

^b RUSH UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AFRICAN AMERICAN; ARTICLE; CAUCASIAN; CONTROLLED STUDY; DNA SEQUENCE; ETHNIC DIFFERENCE; FEMALE; FIFTH EWING VARIANT GENE; GENE; GENE IDENTIFICATION; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NERVE CELL DIFFERENTIATION; PRIORITY JOURNAL; RISK; SEROTONINERGIC SYSTEM; SUDDEN INFANT DEATH SYNDROME;

AFRICAN AMERICANS; BRAIN; CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; INFANT; INTRONS; MALE; MUTAGENESIS, INSERTIONAL; MUTATION; NEURONS; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEROTONIN; SUDDEN INFANT DEATH;

EID: 34547618803     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3180a725a0     Document Type: Article

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