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Kearns-Sayre syndrome
(phenotype)
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Genetic Markers
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No genes found
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Pathway Enrichment
Most Correlated Biogroups
mitochondrial promoter sequence-specific DNA binding
transcription coactivator binding
BARRIER_CANCER_RELAPSE_NORMAL_SAMPLE_UP
YIH_RESPONSE_TO_ARSENITE_C3
nucleoid
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Mouse Phenotypes - Myopathy
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Most Relevant Literature
Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human…
A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fata…
Multiple endocrinopathies (growth hormone deficiency, autoimmune hypothyroidism and diabetes mellitu…
Kearns-Sayre syndrome: a case report].
Kearns Sayre Syndrome--case report with review of literature.
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Natural History of Pearson Syndrome
Genomic Profiling of Mitochondrial Disease - Imaging Analysis for Precise Mitochondrial Medicine
Global Registry and Natural History Study for Mitochondrial Disorders
Inherited Retinal Degenerative Disease Registry
A Long-term Extension of Study RP103-MITO-001 (NCT02023866) to Assess Cysteamine Bitartrate Delayed-…
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