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bibliographicCitation Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation. Auris Nasus Larynx. 2005 Jun;32(2):119–24. doi: 10.1016/j.anl.2005.01.010. PMID: 15917167.
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title Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation
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