Genomic risk factors in sudden infant death syndrome.

Genome Med · 2010 · PMC3016628 · PMID 21122164

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highly significantno p-value reported

[ 28 ] reported in 20 SIDS cases a highly significant interaction between the 5-HTT L allele and polymorphisms in the gene encoding the neurotransmitter inactivator monamine oxidase A ( MAOA ), suggesting the two genotypes act synergistically in modulating SIDS risk.

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