Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome

Neurogenetics

Volumn 12, Issue 1, 2011, Pages 91-92

  Filonzi, Laura ^a   Magnani, Cinzia ^a   Nonnis Marzano, Francesco ^a  

^a UNIVERSITY OF PARMA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; NEUROTRANSMITTER; SEROTONIN TRANSPORTER;

CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; HUMAN; INFANT; LETTER; MALE; PRIORITY JOURNAL; STILLBIRTH; SUDDEN INFANT DEATH SYNDROME; X CHROMOSOMAL INHERITANCE;

ALLELES; CASE-CONTROL STUDIES; FEMALE; GENE FREQUENCY; HUMANS; INFANT; INFANT, NEWBORN; MINISATELLITE REPEATS; MONOAMINE OXIDASE; POLYMORPHISM, GENETIC; PREGNANCY; STILLBIRTH; SUDDEN INFANT DEATH;

EID: 79951550471     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-010-0257-2     Document Type: Letter

References (2)

1. L Filonzi C Magnani AM Lavezzi G Rindi S Parmigiani G Bevilacqua L Matturri F Nonnis Marzano 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 1 65 72 1:CAS:528:DC%2BD1MXotVCisA%3D%3D 10.1007/s10048-008-0149-x 18810510
2. M Klintschar C Heimbold 2010 Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome Neurogenetics 11 367 368 10.1007/s10048-010-0242-9 20354746