Connexin 26 (GJB2) Mutations Associated with Congenital Hearing Loss in a Country of Different Migration Routes: Turkey
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology,Surgery
Link
https://link.springer.com/content/pdf/10.1007/s12070-023-03672-x.pdf
Reference26 articles.
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2. Morton CC, Nance WE (2006) Newborn hearing screening a silent revolution. N Engl J Med 354:2151–2164
3. Lima GM, Marba ST, Santos MF (2006) Hearing screening in a neonatal intensive care unit. J Pediatr (Rio J) 82:110–114
4. Rohlfs AK, Friedhoff J, Bohnert A et al (2017) Unilateral hearing loss in children: a retrospective study and a review of the current literature. Eur J Pediatr 176:475–486
5. Küçük Kurtulgan H, Altuntaş EE, Yıldırım ME et al (2019) The analysis of GJB2, GJB3, and GJB6 gene mutations in patients with hereditary non-syndromic hearing loss living in sivas. J Int Adv Otol 15(3):373–378
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