Identification of a Novel Pathogenic OTOF Variant Causative of Nonsyndromic Hearing Loss With High Frequency in the Ashkenazi Jewish Population

The Application of Clinical Genetics - New Zealand
doi 10.2147/tacg.s113828
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Informa UK Limited

Related search

The R245X Mutation of PCDH15 in Ashkenazi Jewish Children Diagnosed With Nonsyndromic Hearing Loss Foreshadows Retinitis Pigmentosa

Pediatric Research
Child HealthPediatricsPerinatology
2004English

Screening of Connexin 26 in Nonsyndromic Hearing Loss

International Archives of Otorhinolaryngology
Otorhinolaryngology
2014English

Cost-Effectiveness of Population Based BRCA Testing With Varying Ashkenazi Jewish Ancestry

American Journal of Obstetrics and Gynecology
GynecologyObstetrics
2017English

Signatures of Founder Effects, Admixture, and Selection in the Ashkenazi Jewish Population

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2010English

Presymptomatic Diagnosis of Nonsyndromic Hearing Loss by Genotyping

Archives of Otolaryngology–Head & Neck Surgery
1998English

Noncoding Mutations of HGF Are Associated With Nonsyndromic Hearing Loss, DFNB39

American Journal of Human Genetics
Genetics
2009English

Esteem Treatment of Profound High-Frequency Hearing Loss

Otolaryngology - Head and Neck Surgery
OtorhinolaryngologySurgery
2010English

Comprehensive Analysis of Deafness Genes in Families With Autosomal Recessive Nonsyndromic Hearing Loss

PLoS ONE
Multidisciplinary
2015English

A Novel ABCC6 Variant Causative of Pseudoxanthoma Elasticum

Human Genome Variation
BiochemistryGeneticsMolecular Biology
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy