Publication | Closed Access
Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family
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Citations
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References
2006
Year
BiologyChinese FamilyMendelian DisorderGenetic DisorderGeneticsAudiologyRrna A827g MutationAuditory PhysiologyMolecular GeneticsAuditory ResearchAuditory ScienceHuman HearingArtsMedicineMitochondrial 12SHearing Loss
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