Whole-Exome Sequencing to Identify the Cause of Congenital Sensorineural Hearing Loss in Carriers of a Heterozygous GJB2 Mutation
European Archives of Oto-Rhino-Laryngology - Germany
doi 10.1007/s00405-017-4699-0
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Date
August 18, 2017
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Springer Science and Business Media LLC