Article ID Journal Published Year Pages File Type
5714811 International Journal of Pediatric Otorhinolaryngology 2017 16 Pages PDF
Abstract
Our data confirms the phenotype-directed genotyping for DFNB21 deafness against the typical profound HL phenotype seen in the most families segregating ARNSHL. We recommend mutation screening of TECTA in ARNSHL families segregating moderate to severe HL phenotype.
Related Topics
Health Sciences Medicine and Dentistry Otorhinolaryngology and Facial Plastic Surgery
Authors
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