Publication | Open Access
Identical Mitochondrial DNA Deletion in a Woman with Ocular Myopathy and in Her Son with Pearson Syndrome
87
Citations
21
References
2002
Year
Mitochondrial MyopathyGenetic TestingMendelian DisorderMitochondrial FunctionOphthalmologyGenetic DisorderGeneticsOcular MyopathyDna ReplicationLeber Hereditary Optic NeuropathyPathologyPearson SyndromeMolecular GeneticsMedicine
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