Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder.AuthorsAbdel-Salam, Ghada M.H.; Miyake, Noriko; Eid, Maha M.; Abdel-Hamid, Mohamed S.; Hassan, Nihal A.; Eid, Ola M.; Effat, Laila K.; El-Badry, Tarek H.; El-Kamah, Ghada Y.; El-Darouti, Mohamed; Matsumoto, NaomichiPublicationAmerican Journal of Medical Genetics. Part A, 2011, Vol 155A, Issue 11, p2885ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.34299