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Impaired prohormone processing: a grand unified theory for features of Prader-Willi syndrome?
Prader-Willi syndrome (PWS) is a complex disorder that manifests with an array of phenotypes, such as hypotonia and difficulties in feeding during infancy and reduced energy expenditure, hyperphagia, and developmental delays later in life. While the genetic cause has long been known, it is still not...
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| Publicado en: | J Clin Invest |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Society for Clinical Investigation
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5199707/ https://ncbi.nlm.nih.gov/pubmed/27941250 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI91307 |
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