Associated Papers
Panhypopituitarism: genetic versus acquired etiological factors.
Coya R et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2007
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
Turton JP et al.
Clinical Endocrinology, 2005
Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
Rainbow LA et al.
Clinical Endocrinology, 2005
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