Molecular basis of ciliary defects caused by variations of an IFT-B subunit IFT81 found in skeletal ciliopathies

Koshi Tasaki

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

^〇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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The 95th Annual Meeting of the Japanese Biochemical Society

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

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