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PDF) Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain
Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation
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Sonntagszeitung 2. Oktober 2011 [pon2d9j97m40]
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Innovative Genomic Collaboration Using the GENESIS (GEM.app) Platform - Gonzalez - 2015 - Human Mutation - Wiley Online Library
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PDF) Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation
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