LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity - Concepedia

Concepedia

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LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity

DOI Full Paper Access

25

Citations

47

References

2020

Year

Arnaud Besse, Daniel Brezavar, Jennifer Hanson, Austin Larson, Penelope E. Bonnen

Neurodegenerative DiseasesMitochondrial FunctionGenetic DisorderGeneticsPathologyMolecular GeneticsDominant MutationDisease Gene IdentificationMedicineLonp1 Chaperone Activity

References

	Year	Citations

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