Exome-Wide Meta-Analysis Identifies Rare 3′-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea
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DOI: 10.3389/fgene.2017.00151
Abstract: 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… read more here.
Keywords: associated symptoms; ercc1 cd3eap; symptoms sleep; sleep apnea ... See more keywords