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Q48275976-A3849F67-2D5A-4F15-A358-01240F86D6F4
Q48275976-A3849F67-2D5A-4F15-A358-01240F86D6F4
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http://www.wikidata.org/entity/statement/Q48275976-A3849F67-2D5A-4F15-A358-01240F86D6F4
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
P2860
Q48275976-A3849F67-2D5A-4F15-A358-01240F86D6F4
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http://www.wikidata.org/entity/statement/Q48275976-A3849F67-2D5A-4F15-A358-01240F86D6F4
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b88f6416d1404f88f48f3fb8d56d0c374f85214b
P2860
Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.