{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:22:00Z","timestamp":1787016120579,"version":"build-2736575974"},"reference-count":5,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2025,6,6]],"date-time":"2025-06-06T00:00:00Z","timestamp":1749168000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Dermatology"],"published-print":{"date-parts":[[2025,11]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    We report on a novel pathogenic genetic variant in compound heterozygosis of the\n                    <jats:italic>NIPAL4<\/jats:italic>\n                    gene c.396C&gt;Gp.(Ile132Met); additionally, we comment on key clinical findings that contribute to the expansion of the EKVP phenotype in childhood.\n                  <\/jats:p>","DOI":"10.1111\/pde.15959","type":"journal-article","created":{"date-parts":[[2025,6,6]],"date-time":"2025-06-06T06:13:39Z","timestamp":1749190419000},"page":"1297-1298","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Erythrokeratodermia Variabilis due to a Compound Heterozygous Variants in the\n                    <scp>\n                      <i>NIPAL4<\/i>\n                    <\/scp>\n                    Gene"],"prefix":"10.1111","volume":"42","author":[{"given":"Luis Fernando","family":"S\u00e1nchez\u2010Espino","sequence":"first","affiliation":[{"name":"Dermatology Division, Pediatrics Department Stollery Children's Hospital  Edmonton Alberta Canada"},{"name":"Faculty of Medicine &amp; 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