Search

Author/Creator Luan, Weisha

1. Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis. Issue 8 (31st July 2020)

Authors:
Luan, Weisha; Hao, Chen-Zhi; Li, Jia-Qi; Wei, Qing; Gong, Jing-Yu; Qiu, Yi-Ling; Lu, Yi; Shen, Cong-Huan; Xia, Qiang; Xie, Xin-Bao; Zhang, Mei-Hong; Abuduxikuer, Kuerbanjiang; Li, Zhong-Die; Wang, Li; Xing, Qing-He; Knisely, A S; Wang, Jian-She
Journal:
Journal of medical genetics
Issue:
Volume 58:Issue 8(2021)
Page Start:
514
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search