The circling mutant Pcdh15roda is a new mouse model for hearing loss-Reference-Cited by-同舟云学术

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The circling mutant Pcdh15roda is a new mouse model for hearing loss

Published:2013-11 Issue: Volume:751-752 Page:29-35
ISSN:0027-5107
Container-title:Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis
language:en
Short-container-title:Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Author:

Torres Adriana Amorim,Rzadzinska Agnieszka K.,Ribeiro Andrea Frozino,Silva Daniel Almeida da Silva e,Guénet Jean-Louis,Massironi Sílvia Maria Gomes,Godard Ana Lúcia Brunialti

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology

Reference32 articles.

1. The mechanotransduction machinery of hair cells;Grillet;Sci. Signal.,2009

2. Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening;Schimmente;Genet. Med.,2011

3. Hereditary deafness and phenotyping in humans;Bitner-Glindzicz;Brit. Med. Bull.,2002

4. An update on the genetics of Usher Syndrome;Millán;J. Ophthalmol.,2011

5. Mouse models to study inner ear development and hereditary hearing loss;Friedman;Int. J. Dev. Biol.,2007

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sensorineural hearing loss due to a novel mutation in the PCDH15 gene: A case study;Brain Disorders;2023-03

2. Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: Findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortium;BMC Medical Genomics;2015-08-12

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