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Q33312080-341B1EF8-BB5E-46DC-B791-66D071E42419
Q33312080-341B1EF8-BB5E-46DC-B791-66D071E42419
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33312080-341B1EF8-BB5E-46DC-B791-66D071E42419
MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.
P2860
Q33312080-341B1EF8-BB5E-46DC-B791-66D071E42419
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33312080-341B1EF8-BB5E-46DC-B791-66D071E42419
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wasDerivedFrom
758253cbcd02272a6a9bfb3fbc2c0af180b84a1c
P2860
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment.