Publication | Closed Access
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
116
Citations
50
References
2009
Year
BiologyMendelian DisorderRrna 1555AMitochondrial HaplotypesGenetic DisorderGeneticsMolecular GeneticsDisease Gene IdentificationCochlear DevelopmentMedicineG MutationHearing Loss
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