Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss.

Conclusion: These results explain the negligible prevalence of selected mutations among Iranian patients. Identifying common mutations in patients of an ethnic group can reduce the financial costs and time needed for identifying the causes of deafness. PMID: 31997689 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31997689?dopt=Abstract

Source: Fetal and Pediatric Pathology - January 31, 2020 Category: Pathology Tags: Fetal Pediatr Pathol Source Type: research