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non-syndromic hearing loss
- Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairmentKevin T Booth, Kimia Kahrizi, Hossein Najmabadi, Hela Azaiez, Richard JH SmithJournal of Medical Genetics Aug 2018, 55 (8) 555-560; DOI: 10.1136/jmedgenet-2018-105349
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