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Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report

Crossref DOI link: https://doi.org/10.1186/s12881-017-0511-7

Published Online: 2017-12-19

Published Print: 2017-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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