Literature DB >> 16691588

3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis.

Brion S Maher, Mary L Marazita, Casey Rand, Lili Zhou, Elizabeth M Berry-Kravis, Debra E Weese-Mayer.   

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Year:  2006        PMID： 16691588     DOI： 10.1002/ajmg.a.31261

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  4 in total

1.  Tragic and sudden death. Potential and proven mechanisms causing sudden infant death syndrome.

Authors:  Bradley Thach
Journal:  EMBO Rep       Date:  2008-02       Impact factor: 8.807

Review 2.  Gene variants predisposing to SIDS: current knowledge.

Authors:  Siri H Opdal; Torleiv O Rognum
Journal:  Forensic Sci Med Pathol       Date:  2010-07-11       Impact factor: 2.007

Review 3.  Serotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome.

Authors:  David S Paterson
Journal:  Respir Physiol Neurobiol       Date:  2013-07-10       Impact factor: 1.931

Review 4.  Medullary serotonin defects and respiratory dysfunction in sudden infant death syndrome.

Authors:  David S Paterson; Gerard Hilaire; Debra E Weese-Mayer
Journal:  Respir Physiol Neurobiol       Date:  2009-05-27       Impact factor: 1.931
  4 in total

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