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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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| Autori principali: | , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Endocrine Society
2009
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| Soggetti: | |
| Accesso online: | 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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