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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2009
Témata:
Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky