Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression.

By Thönnissen Eva   Rabionet Raquel   Arbonès Maria   Estivill Xavier   Willecke Klaus   Ott Thomas  

Human Genetics, Vol. 111, Iss. 2, 2002-08 ,pp. : 190-197

Springer Publishing Company

Access to resources Recommend Favorite

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

By Liu Xue-Zhong  

Human Molecular Genetics, Vol. 9, Iss. 1, 2000-01 ,pp. : 63-67

Oxford University Press

Access to resources Recommend Favorite

Novel mutations in the connexin43 () and pseudogene may contribute to nonsyndromic hearing loss

By Hong Hui-Mei   Yang Jiann-Jou   Shieh Jia-Ching   Li Mei-Ling   Li Shuan-Yow  

Human Genetics, Vol. 127, Iss. 5, 2010-05 ,pp. : 545-551

Springer Publishing Company

Access to resources Recommend Favorite

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

By Teubner Barbara  

Human Molecular Genetics, Vol. 12, Iss. 1, 2003-01 ,pp. : 13-21

Oxford University Press

Access to resources Recommend Favorite

Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

By Fukuoka Hisakuni   Kanda Yukihiko   Ohta Shuji   Usami Shin-ichi  

Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 510-515

Springer Publishing Company

Access to resources Recommend Favorite