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Q48275976-9C62F6F8-2400-4046-B975-E02B51AB653F
Q48275976-9C62F6F8-2400-4046-B975-E02B51AB653F
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Statement
http://www.wikidata.org/entity/statement/Q48275976-9C62F6F8-2400-4046-B975-E02B51AB653F
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
P2860
Q48275976-9C62F6F8-2400-4046-B975-E02B51AB653F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48275976-9C62F6F8-2400-4046-B975-E02B51AB653F
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Statement
wasDerivedFrom
b88f6416d1404f88f48f3fb8d56d0c374f85214b
P2860
Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.