Ageing contributes to phenotype transition in a mouse model of periodic paralysis

BACKGROUND: Periodic paralysis (PP) is a rare genetic disorder in which ion channel mutation causes episodic paralysis in association with hyper‐ or hypokalaemia. An unexplained but consistent feature of PP is that a phenotype transition occurs around the age of 40, in which the severity of potassiu...

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Detalles Bibliográficos
Autores principales: Suetterlin, Karen J., Tan, S. Veronica, Mannikko, Roope, Phadke, Rahul, Orford, Michael, Eaton, Simon, Sayer, Avan A., Grounds, Miranda D., Matthews, Emma, Greensmith, Linda, Hanna, Michael G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837191/
https://www.ncbi.nlm.nih.gov/pubmed/35174322
http://dx.doi.org/10.1002/rco2.41

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837191/
https://www.ncbi.nlm.nih.gov/pubmed/35174322
http://dx.doi.org/10.1002/rco2.41

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