[P2-04] Poster Session 2-04　Mendelian Disorders

[P2-04-2] Pathology of mice carrying exon 21-skipping variant of Slc12a2, a responsible gene of hereditary hearing loss DFNA78

Hideki Mutai^1,2, Yukiko Kuroda³, Shinobu Noji³, Saki Ichikawa^4,5,8, Koichi Matsuo³, Satoshi Tanaka⁵, Naoyuki Kataoka⁵, Masato Fujioka^1,6, Tatsuo Matsunaga^2,7 (1.Molecular Genetics, Kitasato Univ. School of Medicine, Kanagawa, Japan, 2.National Institute of Sensory Organs, NHO Tokyo Medical Center, Tokyo, Japan, 3.Lab. Cell and Tissue Biology, Keio Univ. School of Medicine, Tokyo, Japan, 4.Dept. Biophysics and Biochemistry, Faculty of Science, Univ. Tokyo, Tokyo, Japan, 5.Lab. Cellular Biochemistry Dept. Animal Resource Sciences / Veterinary Medical Sciences, Graduate School of Agricultural and Life Sceinces, Univ. Tokyo, Tokyo, Japan, 6.Keio University Regenerative Medicine Research Center, Tokyo, Japan, 7.Medical Genetics Center, NHO Tokyo Medical Center, Tokyo, Japan, 8.Graduate School of Pharmaceutical Sciences, Univ. Tokyo, Tokyo, Japan)

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