Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages

Progressive familial intrahepatic cholestasis type 1 (PFIC1), a rare inherited recessive disease resulting from a genetic deficiency in ATP8B1, progresses to liver failure. Because of the difficulty of discriminating PFIC1 from other subtypes of PFIC based on its clinical and histological features a...

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Detalles Bibliográficos
Autores principales: Hayashi, Hisamitsu, Naoi, Sotaro, Togawa, Takao, Hirose, Yu, Kondou, Hiroki, Hasegawa, Yasuhiro, Abukawa, Daiki, Sasaki, Mika, Muroya, Koji, Watanabe, Satoshi, Nakano, Satoshi, Minowa, Kei, Inui, Ayano, Fukuda, Akinari, Kasahara, Mureo, Nagasaka, Hironori, Bessho, Kazuhiko, Suzuki, Mitsuyoshi, Kusuhara, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828058/
https://www.ncbi.nlm.nih.gov/pubmed/29104077
http://dx.doi.org/10.1016/j.ebiom.2017.10.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828058/
https://www.ncbi.nlm.nih.gov/pubmed/29104077
http://dx.doi.org/10.1016/j.ebiom.2017.10.007

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