HIGHLIGHTS
- who: Report and collaborators from the (UNIVERSITY) have published the article: Review began 10/29/2022 Review ended 11/11/2022 Published 11/14/2022 u00a9 Copyright, in the Journal: (JOURNAL) of November/14,/2022
- what: This report identifies a newly disease-causing variant in the NARS2 gene and validates NARS2 as a cause of early-onset nonsyndromic sensorineural hearing loss (DFNB94), adding to the genotypic and phenotypic variability of NARS2-associated disease.
- future: More studies are necessary to analyze the exact effects of NARS2 variants on mitochondrial protein synthesis allowing the development . . .
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