A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2–q12.3
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-008-0596-3.pdf
Reference29 articles.
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2. Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, Sabar MF, Sieving P, Riazuddin S, Griffith AJ, Friedman TB, Belyantseva IA, Wilcox ER (2003) PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum Mol Genet 12:3215–3223
3. Dohkan S, Koike A, and Takagi T (2004) Prediction of protein–protein interactions using Support Vector Machines. In: Proceedings of fourth IEEE symposium on bioInformatics and bioEngineering (BIBE2004). IEEE Computer Society, Los Alamitos, pp 576–584
4. Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED (1997) Pendred syndrome is caused by mutations in putative sulphate transporter gene (PDS). Nat Genet 17:411–422
5. Friedman TB, Griffith AJ (2003) Human nonsyndromic sensorineural deafness. Annu Rev Genomics Hum Genet 4:341–402
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1. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01
2. Genetic Hearing Loss and Gene Therapy;Genomics & Informatics;2018-12-31
3. SLC44A4mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss;Human Molecular Genetics;2016-12-23
4. Non-syndromic hearing loss gene identification: A brief history and glimpse into the future;Molecular and Cellular Probes;2015-10
5. A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss;Biochemical and Biophysical Research Communications;2010-06
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