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Published in: Urolithiasis 5/2019

01-10-2019 | Letter to the Editor

Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation

Authors: M. Bargagli, G. Primiano, A. Primiano, J. Gervasoni, A. Naticchia, S. Servidei, G. Gambaro, P. M. Ferraro

Published in: Urolithiasis | Issue 5/2019

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Excerpt

Dear Editor, …
Literature
12.
go back to reference Tanaka K, Takada Y, Matsunaka T et al (2000) Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA. Intern Med Tokyo Jpn 39:249–252CrossRef Tanaka K, Takada Y, Matsunaka T et al (2000) Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA. Intern Med Tokyo Jpn 39:249–252CrossRef
16.
go back to reference Gambaro G, Vezzoli G, Casari G et al (2004) Genetics of hypercalciuria and calcium nephrolithiasis: from the rare monogenic to the common polygenic forms. Am J Kidney Dis 44:963–986CrossRef Gambaro G, Vezzoli G, Casari G et al (2004) Genetics of hypercalciuria and calcium nephrolithiasis: from the rare monogenic to the common polygenic forms. Am J Kidney Dis 44:963–986CrossRef
Metadata
Title
Recurrent kidney stones in a family with a mitochondrial disorder due to the m.3243A>G mutation
Authors
M. Bargagli
G. Primiano
A. Primiano
J. Gervasoni
A. Naticchia
S. Servidei
G. Gambaro
P. M. Ferraro
Publication date
01-10-2019
Publisher
Springer Berlin Heidelberg
Published in
Urolithiasis / Issue 5/2019
Print ISSN: 2194-7228
Electronic ISSN: 2194-7236
DOI
https://doi.org/10.1007/s00240-018-1087-1

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