Article info

Download PDFPDF
Original research
Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis

Authors

  1. Correspondence to Dr Jian-She Wang, The Center for Pediatric Liver Diseases, Children's Hospital, Fudan University, Shanghai, Shanghai, China; jshwang{at}shmu.edu.cn
View Full Text

Citation

Luan W, Hao C, Li J, et al
Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis

Publication history

  • Received November 17, 2019
  • Revised May 28, 2020
  • Accepted June 20, 2020
  • First published July 31, 2020.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.