Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome

Prader‐Willi Syndrome (PWS) is a rare and incurable congenital neurodevelopmental disorder, resulting from the absence of expression of a group of genes on the paternally acquired chromosome 15q11‐q13. Phenotypical characteristics of PWS include infantile hypotonia, short stature, incomplete puberta...

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Detalles Bibliográficos
Autores principales: Correa‐da‐Silva, Felipe, Fliers, Eric, Swaab, Dick F., Yi, Chun‐Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365683/
https://www.ncbi.nlm.nih.gov/pubmed/34156126
http://dx.doi.org/10.1111/jne.12994

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365683/
https://www.ncbi.nlm.nih.gov/pubmed/34156126
http://dx.doi.org/10.1111/jne.12994

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