Understanding the nomenclature of mitochondrial DNA mutations through examples of two specific disease entities: Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes and Leber hereditary optic neuropathy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine,General Nursing
Reference6 articles.
1. The genetics and pathology of mitochondrial disease;Alston;The Journal of Pathology,2017
2. Emerging model systems and treatment approaches for Leber's hereditary optic neuropathy: Challenges and opportunities;Bahr;Biochim Biophys Acta Mol Basis Dis,2020
3. Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel;Dai;Biomed Rep,2018
4. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options;El-Hattab;Molecular Genetics and Metabolism,2015
5. Acute management of a stroke-like episode in MELAS syndrome: What should we know?;González;eNeurologicalSci,2020
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1. Mitochondrial disorders: Understanding mitochondrial DNA point mutations and deletion syndromes;Journal of the American Association of Nurse Practitioners;2022-08
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