Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
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| Title: | Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD). |
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| Authors: | Turton, James P. G.1, Mehta, Ameeta1,2, Raza, Jamal3, Woods, Kathryn S.1, Tiulpakov, Anatoly4, Cassar, Joseph5, Chong, Kling6, Thomas, Paul Q.7, Eunice, Marumudi8, Ammini, Ariachery C.8, Bouloux, Pierre M.9, Starzyk, Jerzy10, Hindmarsh, Peter C.1,2, Dattani, Mehul T.1,2 mdattani@ich.ucl.ac.uk |
| Source: | Clinical Endocrinology. Jul2005, Vol. 63 Issue 1, p10-18. 9p. |
| Database: | Academic Search Ultimate |
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