Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMKRN3 and pubertal timing.AuthorsNiemitz, EmilyAbstractThe article reports a research on the identification of genetic mutations in the imprinted makorin ring finger protein three (MKRN3) located on chromosome 15 in the Prader-Willi syndrome locus, that causes precocious puberty.SubjectsPRADER-Willi syndrome; PRECOCIOUS pubertyPublicationNature Genetics, 2013, Vol 45, Issue 7, p722ISSN1061-4036Publication typeArticleDOI10.1038/ng.2690