The Serotonin-Related FEV Gene Variant in the Sudden Infant Death Syndrome is a Common Polymorphism in the African–American Population

An important subset of the sudden infant death syndrome (SIDS) is associated with multiple serotonergic (5-HT) abnormalities in regions of the medulla oblongata. The mouse ortholog of the fifth Ewing variant gene (FEV) is critical for 5-HT neuronal development. A putatively rare intronic variant [IV...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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 H.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2009
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2802663/
https://ncbi.nlm.nih.gov/pubmed/19707175
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1203/PDR.0b013e3181bd5a31
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