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 (...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2020-11-01
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| Series: | Cells |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4409/9/11/2446 |