Erblich-bedingte Schwerhörigkeit – Rolle von P2RX2-Genmutationen-Reference-Cited by-同舟云学术

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Erblich-bedingte Schwerhörigkeit – Rolle von P2RX2-Genmutationen

Published:2020-10-27 Issue:11 Volume:99 Page:756-758
ISSN:0935-8943
Container-title:Laryngo-Rhino-Otologie
language:de
Short-container-title:Laryngorhinootologie

Author:

Publisher

Georg Thieme Verlag KG

Subject

Otorhinolaryngology

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1217-2307.pdf

Reference6 articles.

1. Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Phenotype-Genotype Study;X Z Liu;Laryngoscope,2020

2. Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise;D Yan;Proc Natl Acad Sci U S A,2013

3. Genotype-Phenotype Correlation for Predicting Cochlear Implant Outcome: Current Challenges and Opportunities;A A Eshraghi;Front Genet,2020

4. Clinical characteristics and prognosis of low frequency sensorineural hearing loss without vertigo;A Jung;Acta Otolaryngol,2016

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