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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Detaylı Bibliyografya
Asıl Yazarlar: Hamid, Rizwan, Phillips, John A., Holladay, Cindy, Cogan, Joy D., Austin, Eric D., Backeljauw, Philippe F., Travers, Sharon H., Patton, James G.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Endocrine Society 2009
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Original Article
Online Erişim: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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