A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome

By Kwon Min-Jung   Boo Sung Hyun   Kim Hee-Jin   Cho Yang-Sun   Chung Won-Ho   Hong Sung Hwa  

Acta Oto-Laryngologica, Vol. 129, Iss. 6, 2009-06 ,pp. : 688-693

Informa Healthcare

Access to resources Recommend Favorite

Mutation of the EYA1 Gene in Patients with Branchio-oto Syndrome

By Yashima Takatoshi   Noguchi Yoshihiro   Ishikawa Kinya   Mizusawa Hidehiro   Kitamura Ken  

Acta Oto-Laryngologica, Vol. 123, Iss. 2, 2003-01 ,pp. : 279-282

Informa Healthcare

Access to resources Recommend Favorite

A Comparative Study of Eya1 and Eya4 Protein Function and Its Implication in Branchio-oto-renal Syndrome and DFNA10

By Zhang Yuzhou   Knosp Boyd   Maconochie Mark   Friedman Rick   Smith Richard  

JARO - Journal of the Association for Research in Otolaryngology, Vol. 5, Iss. 3, 2004-09 ,pp. : 295-304

Springer Publishing Company

Access to resources Recommend Favorite

Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation

By Noguchi Yoshihiro   Ito Taku   Nishio Ayako   Honda Keiji   Kitamura Ken  

Acta Oto-Laryngologica, Vol. 131, Iss. 4, 2011-04 ,pp. : 413-418

Informa Healthcare

Access to resources Recommend Favorite

A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss

By Noguchi Yoshihiro   Yashima Takatoshi   Hatanaka Akio   Uzawa Masamichi   Yasunami Michio   Kimura Akinori   Kitamura Ken  

Acta Oto-Laryngologica, Vol. 125, Iss. 11, 2005-11 ,pp. : 1189-1194

Informa Healthcare

Access to resources Recommend Favorite