Article
Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome.
Acta paediatrica (Oslo, Norway : 1992) - 1 Apr 2014
Opdal Siri H, Vege Åshild, Rognum Torleiv O
Abstract excerpt
AIM: The purpose of this study was to investigate common polymorphisms in the genes encoding monoamine oxidase A (MAOA) and serotonin transporter (5-HTT) in Norwegian cases of sudden infant death syndrome (SIDS). This was done to further elucidate the role of genetic variation in these genes and SIDS. METHODS: A variable number of tandem repeat area in the promoter of the MAOA gene and rs25531 in the promoter...
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