A Novel Mutation of SCL26A4 gene in Turkish Family with Pendred Syndrome
Aim: This study aimed to investigate the molecular testing of congenital hearing loss by using next generation sequencing technology. Pendred syndrome (PS) is described by severe bilateral sensorineural hearing loss with goiter. The mutations of SCL26A4 gene can cause PS.Material and Method: We eval...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Mustafa Kemal University
2015-06-01
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| Series: | Mustafa Kemal Üniversitesi Tıp Dergisi |
| Subjects: | |
| Online Access: | http://dergipark.gov.tr/mkutfd/issue/19601/209478?publisher=mku |