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Identification and Functional Characterization of Novel Mutations in the Melanocortin-4 Receptor
OBJECTIVE: Melanocortin-4 receptor (MC4R) deficiency is the most common cause of monogenic obesity. In the present study, we screened the MC4R gene for mutations in a population of overweight and obese children and adolescents. METHOD: Cross-sectional mutation analysis of 112 overweight/obese childr...
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| Yayımlandı: | Obes Facts |
|---|---|
| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
S. Karger AG
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6452105/ https://ncbi.nlm.nih.gov/pubmed/20975296 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000321565 |
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