slc26a4 mutation
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Investigation of DFNB4 SLC26A4 mutation in patients with enlarged vestibular aquaduct

2020 ◽  
Vol 138 ◽  
pp. 110379
Author(s):  
Kubilay Kınoğlu ◽  
Kadir Serkan Orhan ◽  
Hakan Kara ◽  
Oğuz Öztürk ◽  
Beldan Polat ◽  
...  
Keyword(s):  
Slc26a4 Mutation

Genotyping and audiological characteristics of infants with a single-allele SLC26A4 mutation

2019 ◽  
Vol 116 ◽  
pp. 153-158 ◽  
Author(s):  
Xuelei Zhao ◽  
Lihui Huang ◽  
Xueyao Wang ◽  
Xianlei Wang ◽  
Liping Zhao ◽  
...  
Keyword(s):  
Single Allele ◽  
Slc26a4 Mutation

scholarly journals Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA

Medicine ◽  
2015 ◽  
Vol 94 (50) ◽  
pp. e2248 ◽  
Author(s):  
Ya-Jie Lu ◽  
Jun Yao ◽  
Qin-Jun Wei ◽  
Guang-Qian Xing ◽  
Xin Cao
Keyword(s):  
Hearing Loss ◽  
Diagnostic Value ◽  
Mutation Status ◽  
Hereditary Hearing Loss ◽  
Slc26a4 Mutation

Prenatal Diagnosis of SLC26A4 Mutation and Delayed Onset of Hearing Loss

2013 ◽  
Vol 148 (4) ◽  
pp. 705-706 ◽  
Author(s):  
Ayaka J. Iwata ◽  
Janet Dunnell ◽  
Susan J. Norton ◽  
Kathleen C. Y. Sie
Keyword(s):  
Hearing Loss ◽  
Prenatal Diagnosis ◽  
Delayed Onset ◽  
Slc26a4 Mutation

scholarly journals SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

2009 ◽  
Vol 54 (5) ◽  
pp. 266-270 ◽  
Author(s):  
Saima Anwar ◽  
Saima Riazuddin ◽  
Zubair M Ahmed ◽  
Saba Tasneem ◽  
Ateeq-ul-Jaleel ◽  
...  
Keyword(s):  
Mutation Spectrum ◽  
Pendred’S Syndrome ◽  
Slc26a4 Mutation

Long-Term Audiological Feature in Pendred Syndrome Caused by SLC26A4 Mutation

2004 ◽  
Vol 131 (2) ◽  
pp. P302-P302
Author(s):  
Yasuyuki Hashimoto ◽  
Satoshi Iwasaki ◽  
Mitsuyoshi Nagura ◽  
Satoru Takebayashi ◽  
Kunihiro Mizuta ◽  
...  
Keyword(s):  
Pendred Syndrome ◽  
Slc26a4 Mutation
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