The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone
Abstract
:1. Introduction
Patients and Methods
2. Results
3. Discussion
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Petrakis, I.; Drosataki, E.; Stavrakaki, I.; Dermitzaki, K.; Lygerou, D.; Konidaki, M.; Pleros, C.; Kroustalakis, N.; Maragkou, S.; Androvitsanea, A.; et al. The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone. Int. J. Mol. Sci. 2022, 23, 7284. https://doi.org/10.3390/ijms23137284
Petrakis I, Drosataki E, Stavrakaki I, Dermitzaki K, Lygerou D, Konidaki M, Pleros C, Kroustalakis N, Maragkou S, Androvitsanea A, et al. The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone. International Journal of Molecular Sciences. 2022; 23(13):7284. https://doi.org/10.3390/ijms23137284
Chicago/Turabian StylePetrakis, Ioannis, Eleni Drosataki, Ioanna Stavrakaki, Kleio Dermitzaki, Dimitra Lygerou, Myrto Konidaki, Christos Pleros, Nikolaos Kroustalakis, Sevasti Maragkou, Ariadni Androvitsanea, and et al. 2022. "The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone" International Journal of Molecular Sciences 23, no. 13: 7284. https://doi.org/10.3390/ijms23137284