V37I connexin 26 allele in patients with sensorineural hearing loss: Evidence of its pathogenicity

2006 ◽  
Vol 140A (22) ◽  
pp. 2394-2400 ◽  
Author(s):  
C. Huculak ◽  
H. Bruyere ◽  
T. N. Nelson ◽  
F. K. Kozak ◽  
S. Langlois
Keyword(s):  
Hearing Loss ◽  
Sensorineural Hearing Loss ◽  
Sensorineural Hearing ◽  
Connexin 26

De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss

2001 ◽  
Vol 108 (3) ◽  
pp. 269-270 ◽  
Author(s):  
Andreas R Janecke ◽  
Doris Nekahm ◽  
Judith Löffler ◽  
Almut Hirst-Stadlmann ◽  
Thomas Müller ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Sensorineural Hearing Loss ◽  
De Novo ◽  
Sensorineural Hearing ◽  
De Novo Mutation ◽  
Connexin 26

Analysis of Gjb2 (Connexin 26) Mutation in Patients with Congenital Non-Syndromic Sensorineural Hearing Loss

2014 ◽  
Vol 52 (1) ◽  
pp. 1-6
Author(s):  
Emin Kaskalan ◽  
Ebru Etem Onalan ◽  
Irfan Kaygusuz ◽  
Turgut Karlidag ◽  
Erol Keles ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Sensorineural Hearing Loss ◽  
Sensorineural Hearing ◽  
Connexin 26

Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss

2002 ◽  
Vol 61 (6) ◽  
pp. 459-464 ◽  
Author(s):  
L Bason ◽  
T Dudley ◽  
K Lewis ◽  
U Shah ◽  
W Potsic ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Sensorineural Hearing Loss ◽  
Sensorineural Hearing ◽  
Connexin 26

scholarly journals GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review

2002 ◽  
Vol 4 (4) ◽  
pp. 258-274 ◽  
Author(s):  
Aileen Kenneson ◽  
Kim Van Naarden Braun ◽  
Coleen Boyle
Keyword(s):  
Hearing Loss ◽  
Sensorineural Hearing Loss ◽  
Sensorineural Hearing ◽  
Connexin 26
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