ArticleHuman molecular genetics2020
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58.
Karina Lezirovitz et al.PubMed ↗Full text ↗Publisher ↗
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ArticleHuman molecular genetics2020
Karina Lezirovitz et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.