Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleReply.AuthorsCichon, Sven; Kruse, Roland; Nöthen, Markus M.AbstractDiscusses the mutation in the human hairless gene. Emergence of autosomal recessive universal congenital alopecia; Examination of disease nomenclature; Identification of the disease-causing chromosome.SubjectsDISEASES; GENETIC mutation; IDENTIFICATIONPublicationJournal of Investigative Dermatology, 2000, Vol 115, Issue 4, p763ISSN0022-202XPublication typeArticleDOI10.1046/j.1523-1747.2000.00124-3.x