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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Detalles Bibliográficos
Autores principales: Ramos-Molina, Bruno, Molina-Vega, María, Fernández-García, José C., Creemers, John W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027271/
https://www.ncbi.nlm.nih.gov/pubmed/29880780
http://dx.doi.org/10.3390/genes9060288

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027271/
https://www.ncbi.nlm.nih.gov/pubmed/29880780
http://dx.doi.org/10.3390/genes9060288

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