The d3-Growth Hormone (GH) Receptor Polymorphism Is Associated with Increased Responsiveness to GH in Turner Syndrome and Short Small-for-Gestational-Age Children
Author(s) -
Gerhard Binder,
Friederike Baur,
Roland Schweizer,
Michael B. Ranke
Publication year - 2006
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2005-1581
Subject(s) - medicine , turner syndrome , endocrinology , small for gestational age , growth hormone receptor , gestational age , growth hormone , hormone , pregnancy , biology , genetics
A protein polymorphism of the GH receptor (GHR) based on the genomic deletion of exon 3 (d3-GHR) has recently been linked to the magnitude of growth response to high-dose recombinant human GH (rhGH) therapy of short children without GH deficiency.
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