Identification of Hearing Loss-Associated Variants of < em > PTPRQ < /em > , < em > MYO15A < /em > , and < em > SERPINB6 < /em > in Pakistani Families

This study reports the identification of novel disease-causing variants in three known deafness genes and further highlights the genetic heterogeneity of HL in Pakistani population.PMID:33997018 | PMC:PMC8080868 | DOI:10.1155/2021/5584788
Source: Biomed Res - Category: Research Authors: Source Type: research