LHON Plus Due to the Variant m.3460G > A Requires Extensive Investigation and Close Monitoring

Author:

Finsterer JosefORCID,Mehri Sounira

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference4 articles.

1. Leber's hereditary optic neuropathy and hypertrophic cardiomyopathy;Hey;CJC Open,2022

2. The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients;Yang;Front Endocrinol (Lausanne),2021

3. Leber's hereditary optic neuropathy plus causing recurrent myelopathy due to an MT-DN1 mutation at G3635A;Lackey;Case Rep Neurol Med,2022

4. Wolff-Parkinson-White syndrome and noncompaction in Leber's hereditary optic neuropathy due to the variant m.3460G > A;Finsterer;J Int Med Res,2018

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