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Q27317126-B0CCE10C-4CFC-48B8-8643-01FB1891013E
Q27317126-B0CCE10C-4CFC-48B8-8643-01FB1891013E
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http://www.wikidata.org/entity/statement/Q27317126-B0CCE10C-4CFC-48B8-8643-01FB1891013E
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran
P2860
Q27317126-B0CCE10C-4CFC-48B8-8643-01FB1891013E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27317126-B0CCE10C-4CFC-48B8-8643-01FB1891013E
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wasDerivedFrom
02166044b6596a9deada29e04dbd1559f875e2a3
P2860
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment