Proteins and proteases of Prader–Willi syndrome: a comprehensive review and perspectives

Prader–Willi Syndrome (PWS) is a rare complex genetic disease that is associated with pathological disorders that include endocrine disruption, developmental, neurological, and physical problems as well as intellectual, and behavioral dysfunction. In early stage, PWS is characterized by respiratory...

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Detalles Bibliográficos
Autores principales: Basak, Sanjukta, Basak, Ajoy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208313/
https://www.ncbi.nlm.nih.gov/pubmed/35621394
http://dx.doi.org/10.1042/BSR20220610

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208313/
https://www.ncbi.nlm.nih.gov/pubmed/35621394
http://dx.doi.org/10.1042/BSR20220610

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