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.
Format: Artigo
Sprog:Inglês
Udgivet: The Endocrine Society 2009
Fag:
Original Article
Online adgang: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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