A Molecular Basis for Variation in Clinical Severity of Isolated Growth Hormone Deficiency Type II

Context: Dominant-negative GH1 mutations cause familial isolated growth hormone deficiency type II (IGHD II), which is characterized by GH deficiency, occasional multiple anterior pituitary hormone deficiencies, and anterior pituitary hypoplasia. The basis of the variable expression and progression...

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Main Authors: Hamid, Rizwan, Phillips, John A., Holladay, Cindy, Cogan, Joy D., Austin, Eric D., Backeljauw, Philippe F., Travers, Sharon H., Patton, James G.
Formáid: Artigo
Teanga:Inglês
Foilsithe: The Endocrine Society 2009
Ábhair:
Original Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2795644/
https://ncbi.nlm.nih.gov/pubmed/19837935
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2009-0746
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