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Q34779797-0225BC8C-4CBE-4912-AC80-AD11E63B66A1
Q34779797-0225BC8C-4CBE-4912-AC80-AD11E63B66A1
BestRank
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http://www.wikidata.org/entity/statement/Q34779797-0225BC8C-4CBE-4912-AC80-AD11E63B66A1
Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
P2860
Q34779797-0225BC8C-4CBE-4912-AC80-AD11E63B66A1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34779797-0225BC8C-4CBE-4912-AC80-AD11E63B66A1
rank
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type
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wasDerivedFrom
b5d726345af8a3b73105a27858a941940359f2a1
P2860
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family