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We report a case of EBS\u2010MIGR with a novel heterozygous pathogenic mutation in exon 9 (frameshift deletion c.1650delC) and likely benign heterozygous mutation in exon 2 (missense c.591C\u00a0&gt;\u00a0A) of keratin 5. This novel pathogenic mutation in<jats:italic>KRT5<\/jats:italic>expands the molecular spectrum of this rare subtype of EBS.<\/jats:p>","DOI":"10.1111\/pde.14087","type":"journal-article","created":{"date-parts":[[2020,1,22]],"date-time":"2020-01-22T06:54:45Z","timestamp":1579676085000},"page":"358-361","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["A novel mutation of keratin 5 in epidermolysis bullosa simplex with migratory circinate erythema"],"prefix":"10.1111","volume":"37","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9745-1331","authenticated-orcid":false,"given":"Basak","family":"Yalici\u2010Armagan","sequence":"first","affiliation":[{"name":"Department of Dermatology and Venereology Faculty of Medicine Hacettepe University Ankara Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Serkan","family":"Kabacam","sequence":"additional","affiliation":[{"name":"Department of Medical 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University Ankara Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2020,1,21]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2133.2010.10146.x"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1523-1747.2003.12424.x"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1111\/jdv.14005"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jdermsci.2013.08.001"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.2340\/00015555-1691"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.2004.00292.x"},{"issue":"1","key":"e_1_2_6_8_1","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1684\/ejd.2017.3190","article-title":"A novel deletion mutation in the 2B domain of KRT5 in epidermolysis bullosa simplex with childhood\u2010onset migratory circinate erythema","volume":"28","author":"Lee 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