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Q47811506-BEE7029D-667E-4DCF-8FA3-545BFFFF618C
Q47811506-BEE7029D-667E-4DCF-8FA3-545BFFFF618C
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http://www.wikidata.org/entity/statement/Q47811506-BEE7029D-667E-4DCF-8FA3-545BFFFF618C
Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.
P2860
Q47811506-BEE7029D-667E-4DCF-8FA3-545BFFFF618C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47811506-BEE7029D-667E-4DCF-8FA3-545BFFFF618C
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wasDerivedFrom
1f610a6d9f41feb4fee1ac27d3a96aa5d5fac5fd
P2860
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss