Clinical Evaluation of Connexin-26 Gene Mutation in the Development of Hearing Loss in the Kazakh Population
-
Published:2022-01-20
Issue:2
Volume:19
Page:em356
-
ISSN:2516-3507
-
Container-title:Electronic Journal of General Medicine
-
language:
-
Short-container-title:ELECTRON J GEN MED
Author:
Assemov AyatORCID,
Kudaibergenova SauleORCID,
Djarkinbekova GulzakhiraORCID,
Musaev AbdukhalilORCID,
Abdukayumov AbdumannopORCID,
Musayev AbduganiORCID
Publisher
Modestum Publishing Ltd
Reference25 articles.
1. Sloan-Heggen CM, Bierer AO, Shearer AE, Kolbe DL, et al. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Hum Genet. 2016;135(4):441-50. https://doi.org/10.1007/s00439-016-1648-8 PMid:26969326 PMCid:PMC4796320
2. van Beeck Calkoen EA, Engel MSD, van de Kamp JM, Yntema HG, et al. The etiological evaluation of sensorineural hearing loss in children. Eur J Pediatr. 2019;178(8):1195-205. https://doi.org/10.1007/s00431-019-03379-8 PMid:31152317 PMCid:PMC6647487
3. Skvorak Giersch AB, Morton CC. Genetic causes of nonsyndromic hearing loss. Curr Opin Pediatr. 1999;11(6):551-7. https://doi.org/10.1097/00008480-199912000-00014 PMid:10590915
4. Funamura JL. Evaluation and management of nonsyndromic congenital hearing loss. Curr Opin Otolaryngol Head Neck Surg. 2017;25(5):385-9. https://doi.org/10.1097/MOO.0000000000000398 PMid:28682819
5. Shearer AE, Smith RJH. Genetics: Advances in genetic testing for deafness. Curr Opin Pediatr. 2012;24(6):679-86. https://doi.org/10.1097/MOP.0b013e3283588f5e PMid:23042251 PMCid:PMC3694178