Publication | Closed Access
Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies
10
Citations
19
References
2010
Year
Mitochondrial MyopathyMitophagyMendelian DisorderPoint MutationsMitochondrial FunctionMitochondrial EncephalomyopathiesGeneticsPathologyMolecular GeneticsNeuropathologyMedicineChinese Patients
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