Weisha Luan

Publication Activity (10 Years)

Years Active: 2020-2020
Publications (10 Years): 1

Top Topics

Intellectual Disability

Autism Spectrum Disorder

Top Venues

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Weisha Luan, Chen-Zhi Hao, Jia-Qi Li, Qing Wei, Jing-Yu Gong, Yi-Ling Qiu, Yi Lu, Cong-Huan Shen, Qiang Xia, Xin-Bao Xie, Mei-Hong Zhang, Kuerbanjiang Abuduxikuer, Zhong-Die Li, Li Wang, Qing-He Xing, A S Knisely, Jian-She Wang
Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis. Journal of medical genetics 58 (8) (2020)