The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population

Journal of genetics

Asli Sirmaci¹  Mustafa Tekin1¹  Duygu Akcayoz-Duman¹ 

[1] Division of Pediatric Molecular Genetics, Ankara University School of Medicine, Ankara 06100, Turkey$$

关键词: connexin26;    connexin30;    deafness;    gap junctions;    GJB2;    GJB6;    hearing impairment.;   

DOI  :  

学科分类：生物科学（综合）

来源: Indian Academy of Sciences

【 授权许可】

Unknown