Characteristics of novel KCNQ4 variants showing a distinct hearing loss phenotype

박미나 – (2017) Characteristics of novel KCNQ4 variants showing a distinct hearing loss phenotype… [8]. Molecular genetic diagnosis Targeted exon sequencing of 129 reported deafness genes (TES-129) from two subjects (SB62-110 and SB155-271) was performed by Otogenetics (Norcross, GA, USA). The acquired reads were aligned Page 12. 3