A genetic perspective on infant mortality.
Causey, Tahnee N; Bodurtha, Joann N; Ford, Nancy.
South Med J
; 103(5): 440-4; quiz 445-6, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20375941
SCN1A variants associated with sudden infant death syndrome.
Comment on Fard et al.'s Candidate gene variants of the immune system and sudden infant death syndrome.
Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?
Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
The genetic autopsy.
Functional significance of channelopathy gene variants in unexplained death.
Multiple genetic variations in sodium channel subunits in a case of sudden infant death syndrome.
Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).
Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.
Monoamine oxidase A gene polymorphism and the pathogenesis of sudden infant death syndrome.