[1P-2] Poster Presentation

4. 高次生命現象・疾患 - l. 遺伝性疾患

[1P-915] Model mice of hereditary hearing loss DFNA78 and species-specific splicing property of the causative gene, SLC12A2

○Hideki Mutai^1,2, Saki Ichikawa^3,4,5, Yukiko Kuroda⁶, Shinobu Noji⁶, Koichi Matsuo⁶, Satoshi Tanaka³, Naoyuki Kataoka³, Masato Fujioka¹, Tatsuo Matsunaga^2,7 (1. Molecular Genetics, Kitasato University School of Medicine, 2. National Institute of Sensory Organs, NHO Tokyo Medical Center, 3. Lab. Cellular Biochemistry, Department of Animal Resource Sciences/ Veterinary Medical Sciences, Graduate School of Agriculture and Life Sciences, The University of Tokyo, 4. Dept. Biophysics and Biochemistry, Faculty of Science, The University of Tokyo, 5. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 6. Lab. Cell and Tissue Biology, Keio University School of Medicine, 7. Center of Clinical Genetics, NHO Tokyo Medical Center)

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