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Sequencing of exons 4, 5, 12 of COCH gene in patients with postlingual sensorineural hearing loss accompanied by vestibular lesion
INTRODUCTION: Mutations at the DFNA9 locus on chromosome 14q12 are the third most common form of DFNA hearing loss, which is clinically characterized by late onset (in adulthood) progressive sensorineural hearing loss accompanied by vestibular dysfunction. The aim of the study was to search for COCH...
Autores principales: | Mielczarek, Marzena, Olszewski, Jurek, Pietkiewicz, Piotr |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949911/ https://www.ncbi.nlm.nih.gov/pubmed/29765451 http://dx.doi.org/10.5114/aoms.2016.60094 |
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