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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 5, 2024. (Total: 234130Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Sudden Infant Death and FEV[original query]
Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.
Pediatric research 2007 Aug 62 (2): 180-2.
Rand Casey M, Berry-Kravis Elizabeth M, Zhou Lili, Fan Wenqing, Weese-Mayer Debra
Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population.
Pediatric research 2009 Dec 66 (6): 631-5.
Broadbelt Kevin G, Barger Melissa A, Paterson David S, Holm Ingrid A, Haas Elisabeth A, Krous Henry F, Kinney Hannah C, Markianos Kyriacos, Beggs Alan
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