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Pharmacologic Correction of Dominant‐Negative GH1 Deficiency Causing Mutations
Purpose: Dominant‐negative growth hormone gene (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. We have previously shown that 1...
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| Gepubliceerd in: | Clin Transl Sci |
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| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Blackwell Publishing Inc
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5439858/ https://ncbi.nlm.nih.gov/pubmed/21707947 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1752-8062.2011.00290.x |
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