MELAS syndrome causes, symptoms, diagnosis, treatment & prognosis
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics
MELAS Syndrome | Hereditary Ocular Diseases
Mitochondrial Medicine: Genetic Underpinnings and Disease Modeling Using Induced Pluripotent Stem Cell Technology. - Abstract - Europe PMC
Mitochondrial Encephalomyopathy - an overview | ScienceDirect Topics
MELAS syndrome - Wikipedia
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics
MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity | Journal of Neurology, Neurosurgery & Psychiatry
Mitochondrial Diseases: Causes, Symptoms & Treatment
Characteristics of iPSCs derived from a MELAS patient. (A) The sequence... | Download Scientific Diagram
Gene therapy for primary mitochondrial diseases: experimental advances and clinical challenges | Nature Reviews Neurology
LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation | European Journal of Human Genetics
A) Map of the human mitochondrial genome and the secondary structure... | Download Scientific Diagram
Non-random distribution of mitochondrial m.3243A>G heteroplasmy in human retina and its impact on cellular phenotype | bioRxiv
Current advances in gene therapy of mitochondrial diseases | Journal of Translational Medicine | Full Text
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics
Figure 1 from Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria | Semantic Scholar
MERRF and MELAS: current gene therapy trends and approaches
The MELAS mutation m.3243A>G promotes reactivation of fetal cardiac genes and an epithelial-mesenchymal transition-like program via dysregulation of miRNAs - ScienceDirect
MELAS syndrome causes, symptoms, diagnosis, treatment & prognosis
MELAS Syndrome - Khondrion
Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report | BMC Neurology | Full Text
