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2. Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity

4. Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish

5. A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

6. Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

8. Biallelic variants in KARS1are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish

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