Citations (14)
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H. Kunst, H. Marres, P. Huygen, G. van Camp, F. Joosten & C. Cremers. (1999) Autosomal Dominant Non-syndromal Low-frequency Sensorineural Hearing Impairment Linked to Chromosome 4p16 (DFNA14): Statistical Analysis of Hearing Threshold in Relation to Age and Evaluation of Vestibulo-ocular Functions. Audiology 38:3, pages 165-173.
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Articles from other publishers (9)
Qiong Li, Shujuan Wang, Pengfei Liang, Wei Li, Jian Wang, Bei Fan, Yang Yang, Xiaogang An, Jun Chen & Dingjun Zha. (2022) A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family. BMC Medical Genomics 15:1.
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Ken Op de Beeck, Lut Van Laer & Guy Van Camp. (2012) DFNA5, a Gene Involved in Hearing Loss and Cancer: A Review. Annals of Otology, Rhinology & Laryngology 121:3, pages 197-207.
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Chuan Yu, Xiangming Meng, Shanfang Zhang, Guoping Zhao, Landian Hu & Xiangyin Kong. (2003) A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family. Genomics 82:5, pages 575-579.
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Lut Van Laer, Egbert Huizing & Guy Van Camp. 2003. Genetic Hearing Loss. Genetic Hearing Loss.
Diederick A. Van Zuijlen, Patrick L. M. Huygen, Els M. R. De Leenheer, Lut Van Laer, Egbert H. Huizing, Guy Van Camp & W. R. J. Cremers. (2016)
Further Delineation of the
DFNA5
Phenotype: Results of Speech Recognition Tests
. Annals of Otology, Rhinology & Laryngology 111:7, pages 639-641.
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Stefano Berrettini, Francesca Ravecca, Stefano Sellari-Franceschini, Fabio Matteucci, Gabriele Siciliano & Francesco Ursino. (1999) Progressive sensorineural hearing loss in childhood. Pediatric Neurology 20:2, pages 130-136.
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Lut Van Laer, Egbert H. Huizing, Margriet Verstreken, Diederick van Zuijlen, Jan G. Wauters, Paul J. Bossuyt, Paul Van de Heyning, Wyman T. McGuirt, Richard J.H. Smith, Patrick J. Willems, P. Kevin Legan, Guy P. Richardson & Guy Van Camp. (1998) Nonsyndromic hearing impairment is associated with a mutation in DFNA5. Nature Genetics 20:2, pages 194-197.
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Paul Coucke, Guy Van Camp, Bulantrisna Djoyodiharjo, Shelley D. Smith, Rune R. Frants, Georges W. Padberg, John K. Darby, Egbert H. Huizing, Cor Cremers, William J. Kimberling, Ben A. Oostra, Paul H. Van de Heyning & Patrick J. Willems. (1994) Linkage of Autosomal Dominant Hearing Loss to the Short Arm of Chromosome 1 in Two Families. New England Journal of Medicine 331:7, pages 425-431.
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Agnete Parving. (1988) Longitudinal study of hearing-disabled children. A follow-up investigation. International Journal of Pediatric Otorhinolaryngology 15:3, pages 233-244.
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