A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy - Concepedia

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A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy

DOI Full Paper Access

32

Citations

7

References

2003

Year

Masakazu Mimaki, Akemi Ikota, Aya Sato, Hirofumi Komaki, Jun Akanuma, Ikuya Nonaka, Yoshihisa Goto

Journal of Human Genetics

BiologyMendelian DisorderMitochondrial FunctionGenetic DisorderNatural SciencesGeneticsMolecular BiologyLeber Hereditary Optic NeuropathyDna ReplicationMolecular GeneticsMedicineHereditary Optic NeuropathyMitochondrial DnaDouble Mutation

References

	Year	Citations

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