@Article{Kalińska-Bienias2016,
journal="Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii",
issn="1642-395X",
volume="33",
number="2",
year="2016",
title="The EVER genes – the genetic etiology of carcinogenesis in epidermodysplasia verruciformis and a possible role in non-epidermodysplasia verruciformis patients",
abstract="In recent years, the two adjacent novel  EVER1  and  EVER2  genes have been identified, whose mutations are responsible for the development of epidermodysplasia verruciformis (EV). Epidermodysplasia verruciformis is a rare, autosomal recessive genodermatosis associated with increased risk of skin carcinoma. Up to now 7 mutations in the  EVER1  gene and 5 mutations in the  EVER2  gene have been identified only in EV. It was also determined that the EVER genes belong to a novel gene family, the transmembrane channel-like (TMC) family, and are responsible for properly functioning zinc homeostasis. These observations have given new insights into EV pathogenesis.",
author="Kalińska-Bienias, Agnieszka
and Kowalewski, Cezary
and Majewski, Sławomir",
pages="75--80",
doi="10.5114/ada.2016.59145",
url="http://dx.doi.org/10.5114/ada.2016.59145"
}