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    Article

    A new mutation in the growth hormone-releasing hormone receptor gene in two Israeli Arab families

    Background: Mutations in the GHRH receptor gene (GHRH-R) are emerging as a common cause of familial isolated GH deficiency (IGHD). Design: We searched for GHRH-R mutations in 10 patients with IGH...

    O. Haskin, L. Lazar, L. Jaber, R. Salvatori in Journal of Endocrinological Investigation (2006)