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Cited by in CrossRef
For: Li LT, Zhao J, Chen R, Wang JS. Two novel VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China. World J Gastroenterol 2014; 20(1): 326-329 [PMID: 24415890 DOI: 10.3748/wjg.v20.i1.326]
URL: https://www.wjgnet.com/1007-9327/full/v20/i1/326.htm
Number Citing Articles
1
Lianhu Yu, Dan Li, Ting Zhang, Yongmei Xiao, Yizhong Wang, Ting Ge. One case of arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome featuring an incomplete and mild phenotypeBMC Nephrology 2022; 23(1) doi: 10.1186/s12882-022-02851-2
2
Jan van der Beek, Caspar Jonker, Reini van der Welle, Nalan Liv, Judith Klumperman. CORVET, CHEVI and HOPS – multisubunit tethers of the endo-lysosomal system in health and diseaseJournal of Cell Science 2019; 132(10) doi: 10.1242/jcs.189134
3
Neng-Li Wang, Yi Lu, Jing-Yu Gong, Xin-Bao Xie, Jing Lin, Kuerbanjiang Abuduxikuer, Mei-Hong Zhang, Jian-She Wang. Molecular findings in children with inherited intrahepatic cholestasisPediatric Research 2020; 87(1): 112 doi: 10.1038/s41390-019-0548-8
4
Yaoyao Zhou, Junfeng Zhang. Arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome: from molecular genetics to clinical featuresItalian Journal of Pediatrics 2014; 40(1) doi: 10.1186/s13052-014-0077-3
5
Yi‐Ling Qiu, Teng Liu, Kuerbanjiang Abuduxikuer, Chen‐Zhi Hao, Jing‐Yu Gong, Mei‐Hong Zhang, Li‐Ting Li, Yan‐Yan Yan, Jia‐Qi Li, Jian‐She Wang. Novel missense mutation in VPS33B is associated with isolated low gamma‐glutamyltransferase cholestasis: Attenuated, incomplete phenotype of arthrogryposis, renal dysfunction, and cholestasis syndrome Human Mutation 2019; 40(12): 2247 doi: 10.1002/humu.23770