Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis.AuthorsLolas, I.B.; Sommerlund, M.; Okkels, H.; Ramsing, M.; Petersen, M.B.AbstractA letter to the editor is presented regarding a novel deletion mutation in the ALOX12B gene in Kurdish patients with autosomal recessive congenital ichthyosis (ARCI).SubjectsHUMAN deletion mutation; ICHTHYOSIS; SKIN disease geneticsPublicationJournal of the European Academy of Dermatology & Venereology, 2016, Vol 30, Issue 11, pe144ISSN0926-9959Publication typeArticleDOI10.1111/jdv.13457