C19orf12 mutation carriers and their first-degree relatives require prospective clinical and genetic work-up
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference7 articles.
1. Retrospective analysis of 17 patients with mitochondrial membrane protein-associated neurodegeneration diagnosed in Russia;Sparber;Park. Relat. Disord.,2021
2. Is there heart disease in cases of neurodegeneration associated with mutations in C19orf12?;Skowronska;Park. Relat. Disord.,2020
3. Retinal and optic nerve abnormalities in neurodegeneration associated with mutations in C19orf12 (MPAN);Langwinska-Wosko;J. Neurol. Sci.,2016
4. Mitochondrial membrane protein-associated neurodegeneration;Gregory,2014
5. Cardiac disease in mitochondrial membrane protein-associated neurodegeneration (MPAN) due to variants in C19orf12;Finsterer;Park. Relat. Disord.,2021
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1. Challenges in the approach and reporting of atypical manifestations of membrane protein-associated neurodegeneration (MPAN): An editorial;Parkinsonism & Related Disorders;2021-08
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