Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?

Title
Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?
Authors
Keywords
-
Journal
European Journal of Medical Genetics
Volume 55, Issue 10, Pages 552-556
Publisher
Elsevier BV
Online
2012-07-07
DOI
10.1016/j.ejmg.2012.06.002

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