[1O05-02] Motor function, Sensory function, Sensory organ

[1O05-02-03] Loss of Smoc1, which encodes an extracellular matrix protein, causes middle and inner ear malformation: Implications for a novel human deafness gene

*Kazuya Ono¹, Yoshifumi Takahata², Tatsuya Katsuno³, Riko Nishimura², Hiroshi Hibino^1,4 (1.The University of Osaka Graduate School of Medicine, 2.The University of Osaka Graduate School of Density, 3.Kyoto University Graduate School of Medicine, 4.The University of Osaka Global Center for Medical Engineering and Informatics,)

Keywords:

rare disease

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