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CC Morton et al.
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T Matsunaga et al.
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T Matsunaga et al.
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S Finnilä et al.
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SG Malik et al.
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E Ostergaard et al.
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Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment
MS Lehtonen et al.
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S Usami et al.
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S Iwasaki et al.
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