Cyclin M2 (CNNM2) knockout mice show mild hypomagnesaemia and developmental defects

Patients with mutations in Cyclin M2 (CNNM2) suffer from hypomagnesaemia, seizures, and intellectual disability. Although the molecular function of CNNM2 is under debate, the protein is considered essential for renal Mg(2+) reabsorption. Here, we used a Cnnm2 knock out mouse model, generated by CRIS...

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Detalles Bibliográficos
Autores principales: Franken, Gijs A. C., Seker, Murat, Bos, Caro, Siemons, Laura A. H., van der Eerden, Bram C. J., Christ, Annabel, Hoenderop, Joost G. J., Bindels, René J. M., Müller, Dominik, Breiderhoff, Tilman, de Baaij, Jeroen H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050252/
https://www.ncbi.nlm.nih.gov/pubmed/33859252
http://dx.doi.org/10.1038/s41598-021-87548-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050252/
https://www.ncbi.nlm.nih.gov/pubmed/33859252
http://dx.doi.org/10.1038/s41598-021-87548-6

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