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SNP Linkage Analysis and Whole Exome Sequencing Identify a Novel POU4F3 Mutation in Autosomal Dominant Late-Onset Nonsyndromic Hearing Loss (DFNA15)
- Hee-Jin Kim,
- Hong-Hee Won,
- Kyoung-Jin Park,
- Sung Hwa Hong,
- Chang-Seok Ki,
- Sang Sun Cho,
- Hanka Venselaar,
- Gert Vriend,
- Jong-Won Kim
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- Published: November 18, 2013
- https://doi.org/10.1371/journal.pone.0079063