Laron Syndrome Research Paves the Way for New Insights in Oncological Investigation
Laron syndrome (LS) is a rare genetic endocrinopathy that results from mutation of the growth hormone receptor (<i>GH-R</i>) gene and is typically associated with dwarfism and obesity. LS is the best characterized entity under the spectrum of the congenital insulin-like growth factor-1 (IGF1) defici...
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| Principais autores: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI AG
2020-11-01
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| Serija: | Cells |
| Teme: | |
| Online dostop: | https://www.mdpi.com/2073-4409/9/11/2446 |
| Oznake: |
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