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Referenzen:
[1] Courts, C., Grabmüller, M., & Madea, B. (2013). Monoamine Oxidase A Gene Polymorphism and the Pathogenesis of Sudden Infant Death Syndrome The Journal of Pediatrics DOI: 10.1016/j.jpeds.2012.12.072
Filonzi L, Magnani C, Lavezzi A M, Rindi G, Parmigiani S, Bevilacqua G, Matturri L, & Nonnis-Marzano F (2009). Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis. Neurogenetics. 10: 65-72.
Filonzi L, Magnani C, & Nonnis-Marzano F (2011). Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome. Neurogenetics. 12: 91-92.
Klintschar M & Heimbold C (2010). Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome. Neurogenetics. 11: 367-368.
Klintschar M & Heimbold C (2012). Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome. Pediatrics 129: e756-e761.
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