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Hyperphagia and Obesity in Prader–Willi Syndrome: PCSK1 Deficiency and Beyond?
Prader–Willi syndrome (PWS) is a complex genetic disorder that, besides cognitive impairments, is characterized by hyperphagia, obesity, hypogonadism, and growth impairment. Proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency, a rare recessive congenital disorder, partially overlaps phe...
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| Publicado no: | Genes (Basel) |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6027271/ https://ncbi.nlm.nih.gov/pubmed/29880780 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes9060288 |
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