(PDF) Leigh Syndrome Caused by the MT-ND5 M.13513G>A

Leigh Syndrome Caused by the MT-ND5 M.13513G>A Mutation: A Case Presenting With WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia

JIMD Reports - Germany

doi 10.1007/8904_2014_375

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January 1, 2014

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Springer Berlin Heidelberg

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Leigh Syndrome Caused by the MT-ND5 M.13513G>A Mutation: A Case Presenting With WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia

JIMD Reports - Germany

doi 10.1007/8904_2014_375

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome

A Case Concealed WPW Syndrome With Enhanced A-H Conduction

Illness-Induced Exacerbation of Leigh Syndrome in a Patient With the MTATP6 Mutation, M. 9185 T>C

Septal Myectomy for Severe Neonatal Hypertrophic Cardiomyopathy Caused by PTPN11 Gene Mutation: A Case Report

Primary Electrical Disorder or Primary Cardiomyopathy?: A Case With a Unique Association of Noncompaction Cardiomyopathy and Cathecolaminergic Polymorphic Ventricular Tachycardia Caused by Ryanodine Receptor Mutation

A Case With Infectious Mononucleosis-Like Syndrome Caused by Human Herpes Virus-6 Infection

The Wolff-Parkinson-White (WPW) Syndrome With Supernormal Conduction Through the Anomalous Bypass

A Serine Synthesis Defect Presenting With a Charcot-Marie-Tooth–Like Polyneuropathy

Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation