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[1T09a-03(2P-147)] Molecular basis of ciliary defects caused by variations of an IFT-B subunit IFT81 found in skeletal ciliopathies

Koshi Tasaki1, Yamato Ishida1, Yohei Katoh1, Kazuhisa Nakayama1 (Department of Physiological Chemistry, Graduate School of Pharmaceutical Science, Kyoto University)

キーテクノロジー:ゲノム編集

primary cilia、IFT-B complex、IFT81、ciliopathy

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