Predictive Sensitivity and Concordance of Machine-learning Tools for Diagnosing DFNA9 in a Large Series of p.Pro51Ser Variant Carriers in the COCH-gene-Reference-Cited by-同舟云学术

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Predictive Sensitivity and Concordance of Machine-learning Tools for Diagnosing DFNA9 in a Large Series of p.Pro51Ser Variant Carriers in the COCH-gene

Published:2021-01-22 Issue: Volume:Publish Ahead of Print Page:
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Salah Mahadi,de Varebeke Sebastien Janssens,Fransen Erik,Topsakal Vedat,Van Camp Guy,Van Rompaey Vincent

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Sensory Systems,Otorhinolaryngology

Reference21 articles.

1. The prevalence of hearing impairment and associated risk factors: The Beaver Dam Offspring Study;Nash;Arch Otolaryngol Head Neck Surg,2011

2. Genetic epidemiology of hearing impairment;Morton;Ann N Y Acad Sci,1991

3. Genetics of hearing loss—nonsyndromic;Chang;Otolaryngol Clin North Am,2015

4. Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening;Robertson;Genomics,1994

5. Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH;Bom;Ann Otol Rhinol Laryngol,2003

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