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Insulin resistance and obesity-related factors in Prader–Willi syndrome: Comparison with obese subjects
Prader–Willi syndrome (PWS), the most common genetic cause of marked obesity in humans, is usually due to a de novo paternally derived chromosome 15q11–q13 deletion or maternal disomy 15 [(uniparental disomy (UPD)]. Obesity is due to energy imbalance, but few studies have examined fat patterning and...
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| Publicado no: | Clin Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6704480/ https://ncbi.nlm.nih.gov/pubmed/15691361 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2004.00392.x |
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