Newer variants of progressive familial intrahepatic cholestasis

Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of disorders characterized by defects in bile secretion and presentation with intrahepatic cholestasis in infancy or childhood. The most common types include PFIC 1 (deficiency of FIC1 protein, ATP8B1 gene mutation), PFIC...

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Detalles Bibliográficos
Autores principales: Vinayagamoorthy, Vignesh, Srivastava, Anshu, Sarma, Moinak Sen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Minireviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727216/
https://www.ncbi.nlm.nih.gov/pubmed/35070006
http://dx.doi.org/10.4254/wjh.v13.i12.2024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727216/
https://www.ncbi.nlm.nih.gov/pubmed/35070006
http://dx.doi.org/10.4254/wjh.v13.i12.2024

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