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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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI AG
2020-11-01
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| Series: | Cells |
| Assuntos: | |
| Acceso en liña: | https://www.mdpi.com/2073-4409/9/11/2446 |
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