Küçük Kurtulgan, Hande <br/><br/>
The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.  [electronic resource] 

 -  The journal of international advanced otology  Dec 2019 
 - 373-378 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2148-3817 
<br/><br/><label>Standard No.: </label>10.5152/iao.2019.5401  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Connexin 26<br/>Connexin 30--genetics<br/>Connexins--genetics<br/>Consanguinity<br/>Female<br/>Gene Frequency<br/>Genotype<br/>Hearing Loss, Sensorineural--genetics<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Turkey<br/>Young Adult