Solute carrier 41A3 encodes for a mitochondrial Mg2+ efflux system
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep27999.pdf
Reference45 articles.
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3. Schlingmann, K. P. et al. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family. Nature genetics 31, 166–170, doi: 10.1038/ng889 (2002).
4. Zhou, H. & Clapham, D. E. Mammalian MagT1 and TUSC3 are required for cellular magnesium uptake and vertebrate embryonic development. Proceedings of the National Academy of Sciences of the United States of America 106, 15750–15755, doi: 10.1073/pnas.0908332106 (2009).
5. Kolisek, M., Nestler, A., Vormann, J. & Schweigel-Rontgen, M. Human gene SLC41A1 encodes for the Na+/Mg2+ exchanger. American journal of physiology. Cell physiology 302, C318–326, doi: 10.1152/ajpcell.00289.2011 (2012).
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