A. Ohtsuka

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

G. Camp, S. Usami, S. Abe, 2003, Human Genetics.

Deafness Due to A1555G Mitochondrial Mutation Without Use of Aminoglycoside

T. Matsunaga, S. Usami, M. Shiroma, 2004, The Laryngoscope.

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

G. Otting, E. Fransen, L. Patthy, 2003, European Journal of Human Genetics.

Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns

Satoshi Iwasaki, Tomohiro Oguchi, Takashi Nakagawa, 2005, Journal of Human Genetics.

Identification of 605ins46, a novel GJB2 mutation in a Japanese family.

T. Matsunaga, S. Usami, Isamu Yuge, 2002, Auris, nasus, larynx.