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Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits
Prader–Willi syndrome (PWS) is a genetic disorder characterized by a variety of physiological and behavioral dysregulations, including hyperphagia, a condition that can lead to life-threatening obesity. Feeding behavior is a highly complex process with multiple feedback loops that involve both perip...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5179922/ https://ncbi.nlm.nih.gov/pubmed/27288456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw169 |
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