Differences in circulating microRNA signature in Prader–Willi syndrome and non-syndromic obesity
Prader–Willi syndrome (PWS) represents the most common genetic-derived obesity disorder caused by the loss of expression of genes located on the paternal chromosome 15q11.2-q13. The PWS phenotype shows peculiar physical, endocrine and metabolic characteristics compared to those observed in non-syndr...
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| Principais autores: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Bioscientifica
2018-11-01
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| Series: | Endocrine Connections |
| Assuntos: | |
| Acceso en liña: | https://ec.bioscientifica.com/view/journals/ec/7/12/EC-18-0329.xml |
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