M. Wagatsuma

Distribution and frequencies of CDH23 mutations in Japanese patients with non‐syndromic hearing loss

Y. Takumi, S. Usami, M. Wagatsuma, 2007, Clinical genetics.

The responsible genes in Japanese deafness patients and clinical application using Invader assay

Y. Takumi, S. Nishio, S. Usami, 2008, Acta oto-laryngologica.

A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene.

J. van den Ende, F. Declau, F. Vanhoenacker, 2006, American journal of human genetics.