Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans.
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Mutai H, et al. Among authors: morimoto n.
PLoS Genet. 2020 Apr 15;16(4):e1008643. doi: 10.1371/journal.pgen.1008643. eCollection 2020 Apr.
PLoS Genet. 2020.
PMID: 32294086
Free PMC article.