Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte‐Derived Macrophages
Ayumu Mizutani, Yusuke Sabu, Sotaro Naoi, Shogo Ito, Satoshi Nakano, Kei Minowa, Tatsuki Mizuochi, Koichi Ito, Daiki Abukawa, Shunsaku Kaji, Mika Sasaki, Koji Muroya, Yoshihiro Azuma, Satoshi Watanabe, Yuki Oya, Yukihiro Inomata, Akinari Fukuda, Mureo Kasahara, Ayano Inui, Hajime Takikawa, Hiroyuki Kusuhara, Kazuhiko Bessho, Mitsuyoshi Suzuki, Takao Togawa, Hisamitsu Hayashi – 26 September 2020 – Adenosine triphosphatase phospholipid transporting 8B1 (ATP8B1) deficiency, an ultrarare autosomal recessive liver disease, includes severe and mild clinical forms, referred to as progressive famil