Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD). - Turton, James P. G.; Mehta, Ameeta; Raza, Jamal; Woods, Kathryn S.; Tiulpakov, Anatoly; Cassar, Joseph; Chong, Kling; Thomas, Paul Q.; Eunice, Marumudi; Ammini, Ariachery C.; Bouloux, Pierre M.; Starzyk, Jerzy; et al. (Clinical Endocrinology, 2005)