Caricamento...
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...
Salvato in:
| Pubblicato in: | Clin Genet |
|---|---|
| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2005
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|