Exome-Wide Meta-Analysis Identifies Rare 3′-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea

Obstructive sleep apnea (OSA) is a common sleep breathing disorder associated with an increased risk of cardiovascular and cerebrovascular diseases and mortality. Although OSA is fairly heritable (~40%), there have been only few studies looking into the genetics of OSA. In the present study, we aime...

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Detalles Bibliográficos
Autores principales: van der Spek, Ashley, Luik, Annemarie I., Kocevska, Desana, Liu, Chunyu, Brouwer, Rutger W. W., van Rooij, Jeroen G. J., van den Hout, Mirjam C. G. N., Kraaij, Robert, Hofman, Albert, Uitterlinden, André G., van IJcken, Wilfred F. J., Gottlieb, Daniel J., Tiemeier, Henning, van Duijn, Cornelia M., Amin, Najaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651235/
https://www.ncbi.nlm.nih.gov/pubmed/29093733
http://dx.doi.org/10.3389/fgene.2017.00151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651235/
https://www.ncbi.nlm.nih.gov/pubmed/29093733
http://dx.doi.org/10.3389/fgene.2017.00151

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