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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Hamid, Rizwan, Phillips, John A., Holladay, Cindy, Cogan, Joy D., Austin, Eric D., Backeljauw, Philippe F., Travers, Sharon H., Patton, James G.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The Endocrine Society 2009
Gaiak:
Original Article
Sarrera elektronikoa: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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