Prevalence of early repolarisation pattern in patients with inherited channelopathy

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Link between pain and olfaction in an inherited sodium channelopathy.

In a major breakthrough in our understanding of human olfaction, a recent study showed that loss-of-function mutations in the voltage-gated sodium channel Nav1.7, encoded by the gene SCN9A, cause a loss of the sense of smell (congenital general anosmia) in mice and humans. These findings are of special clinical relevance because Nav1.7 was previously known for its essential role in the percepti...

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ژورنال

عنوان ژورنال: Heart, Lung and Circulation

سال: 2015

ISSN: 1443-9506

DOI: 10.1016/j.hlc.2015.06.679