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Obesity management in Prader–Willi syndrome: current perspectives
Prader–Willi syndrome (PWS) is a complex multisystem disorder due to the absent expression of the paternally active genes in the PWS critical region on chromosome 15 (15q11.2-q13). The syndrome is considered the most common genetic cause of obesity, occurring in 1:10,000–1:30,000 live births. Its ma...
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| Publicat a: | Diabetes Metab Syndr Obes |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6175547/ https://ncbi.nlm.nih.gov/pubmed/30323638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DMSO.S141352 |
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