Publication | Open Access
Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene
102
Citations
41
References
1999
Year
C12258a MutationMendelian DisorderMitochondrial FunctionGenetic DisorderRetinitis PigmentosaGeneticsMolecular BiologyPathologyMitochondrial MedicineMolecular GeneticsCochlear DevelopmentMedicineMitochondrial Mtts2 GeneNeurogenetics
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