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...

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Detalles Bibliográficos
Autores principales: Mielczarek, Marzena, Olszewski, Jurek, Pietkiewicz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Basic Research
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

Internet

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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