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Q30485662-36F9610B-8699-4C90-A0CA-BDB35F0CAC2E
Q30485662-36F9610B-8699-4C90-A0CA-BDB35F0CAC2E
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http://www.wikidata.org/entity/statement/Q30485662-36F9610B-8699-4C90-A0CA-BDB35F0CAC2E
Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.
P2860
Q30485662-36F9610B-8699-4C90-A0CA-BDB35F0CAC2E
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Statement
http://www.wikidata.org/entity/statement/Q30485662-36F9610B-8699-4C90-A0CA-BDB35F0CAC2E
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7300ed71cdf5172a44b4630990482cfb7456c11e
P2860
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss