Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Urology
Link
http://link.springer.com/content/pdf/10.1007/s00240-018-1087-1.pdf
Reference16 articles.
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3. Emma F, Montini G, Parikh SM, Salviati L (2016) Mitochondrial dysfunction in inherited renal disease and acute kidney injury. Nat Rev Nephrol 12:267–280. https://doi.org/10.1038/nrneph.2015.214
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5. Pickett SJ, Grady JP, Ng YS et al (2018) Phenotypic heterogeneity in m.3243A>G mitochondrial disease: the role of nuclear factors. Ann Clin Transl Neurol 5:333–345. https://doi.org/10.1002/acn3.532
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