MELAS reflects a clinical concept with heterogeneous genetic background
Author:
Affiliation:
1. Veterinary University of Vienna, Austria
2. University of Tunis El Manar and Genomics Platform, Tunisia
Publisher
FapUNIFESP (SciELO)
Subject
Neurology,Neurology (clinical)
Link
http://www.scielo.br/pdf/anp/v77n2/1678-4227-anp-77-02-0142.pdf
Reference10 articles.
1. When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?;Lorenzoni PJ;Arq Neuropsiquiatr.,2015
2. MELAS: a nationwide prospective cohort study of 96 patients in Japan;Yatsuga S;Biochim Biophys Acta.,2012
3. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome;Pavlakis SG;Ann Neurol.,1984
4. Clinical perspectives of mitochondrial disorders;Finsterer J;Pediatr Endocrinol Rev.,2018
5. Identification of FASTKD2 compound heterozygous mutations as the underlying cause of autosomal recessive MELAS-like syndrome;Yoo DH;Mitochondrion.,2017
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