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1835
2025

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1835 1
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1988 2
1998 1
1999 6
2000 4
2001 1
2002 5
2003 3
2004 7
2005 5
2006 6
2007 6
2008 4
2009 9
2010 4
2011 3
2012 6
2013 7
2014 6
2015 6
2016 4
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2019 4
2020 2
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2025 0

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A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
Riahi Z, Chahed H, Jaafoura H, Zainine R, Messaoud O, Naili M, Nagara M, Hammami H, Laroussi N, Bouyacoub Y, Kefi R, Bonnet C, Besbes G, Abdelhak S. Riahi Z, et al. Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1485-8. doi: 10.1016/j.ijporl.2013.06.015. Epub 2013 Jul 12. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23856379
Audiological features of GJB2 (connexin 26) deafness.
Liu XZ, Pandya A, Angeli S, Telischi FF, Arnos KS, Nance WE, Balkany T. Liu XZ, et al. Ear Hear. 2005 Jun;26(3):361-9. doi: 10.1097/00003446-200506000-00011. Ear Hear. 2005. PMID: 15937416
130 results