In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing loss

by Namba, Kazunori, Mutai, Hideki, Kaneko, Hiroki, Hashimoto, Sho, Matsunaga, Tatsuo
Published 2012

Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

by Mutai, Hideki, Suzuki, Naohiro, Shimizu, Atsushi, Torii, Chiharu, Namba, Kazunori, Morimoto, Noriko, Kudoh, Jun, Kaga, Kimitaka, Kosaki, Kenjiro, Matsunaga, Tatsuo
Published 2013

High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss

by Mizutari, Kunio, Mutai, Hideki, Namba, Kazunori, Miyanaga, Yuko, Nakano, Atsuko, Arimoto, Yukiko, Masuda, Sawako, Morimoto, Noriko, Sakamoto, Hirokazu, Kaga, Kimitaka, Matsunaga, Tatsuo
Published 2015