We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleExpanding The Phenotypic Spectrum of Cx26 Disorders: Bart–Pumphrey Syndrome is Caused by a Novel Missense Mutation in GJB2AuthorsRichard, Gabriele; Brown, Nkecha; Ishida-Yamamoto, Akemi; Krol, AlfonsPublicationJournal of Investigative Dermatology, 2004, Vol 123, Issue 5, p856ISSN0022-202xPublication typearticleDOI10.1111/j.0022-202x.2004.23470.x