Publication | Closed Access
Clinical and molecular characteristics of newly reported mitochondrial disease entity caused by biallelic PARS2 mutations
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Citations
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References
2018
Year
Mendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseaseBiallelic Pars2 MutationsMolecular BiologyPathologyMitochondrial MedicineMolecular GeneticsMolecular CharacteristicsMitochondrial Disease EntityMedicine
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