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Here we report two siblings with bullous dermolysis of the newborn who were born prematurely and have a novel recessive mutation, p.Pro2259Leu, in the triple helix domain of type <jats:styled-content style=\"fixed-case\">VII<\/jats:styled-content> collagen. We discuss the possible relationship between genotype and prematurity and clinical manifestations in these patients.<\/jats:p>","DOI":"10.1111\/pde.12513","type":"journal-article","created":{"date-parts":[[2015,1,30]],"date-time":"2015-01-30T07:18:23Z","timestamp":1422602303000},"source":"Crossref","is-referenced-by-count":8,"title":["Recessive Bullous Dermolysis of the Newborn in Preterm Siblings with a Missense Mutation in Type <scp>VII<\/scp> Collagen"],"prefix":"10.1111","volume":"32","author":[{"given":"Valeria","family":"Boccaletti","sequence":"first","affiliation":[{"name":"Department of Dermatology Parma University Hospital Parma Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giovanna","family":"Zambruno","sequence":"additional","affiliation":[{"name":"Laboratory of Molecular and Cell Biology Istituto Dermopatico dell'Immacolata\u2010IRCSS Rome 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