Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome

2016 ◽  
Vol 85 ◽  
pp. 75-79 ◽  
Author(s):  
Fengguo Zhang ◽  
Xiaohui Bai ◽  
Yun Xiao ◽  
Xue Zhang ◽  
Guodong Zhang ◽  
...  
Keyword(s):  
Novel Mutation ◽  
Chinese Family ◽  
Enlarged Vestibular Aqueduct ◽  
Vestibular Aqueduct ◽  
Slc26a4 Gene

scholarly journals Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct

2018 ◽  
Vol 12 (5) ◽  
pp. 502-506 ◽  
Author(s):  
Xuelei Zhao ◽  
Xiaohua Cheng ◽  
Lihui Huang ◽  
Xianlei Wang ◽  
Cheng Wen ◽  
...  
Keyword(s):  
Chinese Family ◽  
Compound Heterozygous ◽  
Enlarged Vestibular Aqueduct ◽  
Vestibular Aqueduct ◽  
Compound Heterozygous Mutations ◽  
I Gene

scholarly journals The Influence of Mutations in the SLC26A4 Gene on the Temporal Bone in a Population With Enlarged Vestibular Aqueduct

2007 ◽  
Vol 133 (2) ◽  
pp. 162 ◽  
Author(s):  
Colm Madden ◽  
Mark Halsted ◽  
Jareen Meinzen-Derr ◽  
Dianna Bardo ◽  
Mark Boston ◽  
...  
Keyword(s):  
Temporal Bone ◽  
Enlarged Vestibular Aqueduct ◽  
Vestibular Aqueduct ◽  
Slc26a4 Gene

scholarly journals SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

2006 ◽  
Vol 14 (6) ◽  
pp. 773-779 ◽  
Author(s):  
Sébastien Albert ◽  
Hélène Blons ◽  
Laurence Jonard ◽  
Delphine Feldmann ◽  
Pierre Chauvin ◽  
...  
Keyword(s):  
Hearing Impairment ◽  
Enlarged Vestibular Aqueduct ◽  
Vestibular Aqueduct ◽  
Slc26a4 Gene

scholarly journals SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueduct

2012 ◽  
Vol 10 (1) ◽  
pp. 82 ◽  
Author(s):  
Jiandong Zhao ◽  
Yongyi Yuan ◽  
Jing Chen ◽  
Shasha Huang ◽  
Guojian Wang ◽  
...  
Keyword(s):  
Copy Number ◽  
Gene Copy Number ◽  
Copy Number Variations ◽  
Chinese Patients ◽  
Gene Copy ◽  
Enlarged Vestibular Aqueduct ◽  
Vestibular Aqueduct ◽  
Slc26a4 Gene

A Novel mutation in the SLC26A4 gene in a Chinese family with Pendred syndrome

2013 ◽  
Vol 77 (9) ◽  
pp. 1495-1499 ◽  
Author(s):  
Chun-Jui Huang ◽  
Tsun-Hsing Lei ◽  
Wei-Lun Chang ◽  
Tzong-Yang Tu ◽  
An-Suey Shiao ◽  
...  
Keyword(s):  
Novel Mutation ◽  
Chinese Family ◽  
Pendred Syndrome ◽  
Slc26a4 Gene
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