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Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.

• Authors : Mori, Kentaro; Moteki, Hideaki; Miyagawa, Maiko

• Source: PLoS ONE. September 14, 2016, Vol. 11 Issue 9, e0162230.

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Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.

• Authors : Ahmed, Zubair M.; Riazuddin, Saima; Aye, Sandar

• Source: Human Genetics. October, 2008, Vol. 124 Issue 3, p215, 9 p.

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Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS.

• Authors : Miyagawa, Maiko; Nishio, Shin-ya; Ikeda, Takuo

• Source: PLoS ONE. October 9, 2013, Vol. 8 Issue 10, e75793.

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A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.

• Authors : Pater, Justin A.; Benteau, Tammy; Griffin, Anne

• Source: Human Genetics. January, 2017, Vol. 136 Issue 1, p107, 12 p.

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Novel mutations and the ophthalmologic characters in Chinese patients with Wolfram Syndrome.

• Authors : Zhang, Youjia; Feng, Lili; Kong, Xiangmei

• Source: Orphanet Journal of Rare Diseases. August 7, 2019, Vol. 14 Issue 1.

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Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report.

• Authors : Varga, Lukas; Danis, Daniel; Skopkova, Martina

• Source: BMC Medical Genetics. May 17, 2019, Vol. 20 Issue 1.

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Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study.

• Authors : Usami, Shin-ichi; Nishio, Shin-ya; Nagano, Makoto

• Source: PLoS ONE. February 24, 2012, Vol. 7 Issue 2, e31276.

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SCIENCE WATCH; Hearing Aids for Dogs.

• Source: The New York Times. December 1, 1987.

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Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesis.

• Authors : Rouse, Stephanie L.; Florentine, Michelle M.; Taketa, Emily

• Source: Human Genetics. April, 2022, Vol. 141 Issue 3-4, p485, 10 p.

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Genetic testing for pediatric hearing loss: no time to waste.

• Authors : Kenna, Margaret A.

• Source: Human Genetics. April, 2022, Vol. 141 Issue 3-4, p315, 3 p.

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