Identification of causative variants in patients with non-syndromic hearing loss in the Minnan region, China by targeted next-generation sequencing.

CONCLUSIONS AND SIGNIFICANCE: Our targeted NGS analysis added supports for the application of NGS in routine diagnosis and provided an overview of genetic variants with allele frequencies in the deaf population from the Minnan region. PMID: 30762455 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/30762455?dopt=Abstract

Source: Acta Oto-Laryngologica - February 14, 2019 Category: ENT & OMF Authors: Wu X, Gao X, Han P, Zhou Y Tags: Acta Otolaryngol Source Type: research