Clinical and molecular characterization of four patients with NTCP deficiency from two unrelated families harboring the novel SLC10A1 variant c.595A>C (p.Ser199Arg)-Reference-Cited by-同舟云学术

Clinical and molecular characterization of four patients with NTCP deficiency from two unrelated families harboring the novel SLC10A1 variant c.595A>C (p.Ser199Arg)

Published:2019-10-23 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Li Hua¹,Deng Mei¹,Guo Li¹,Qiu Jian‑Wu¹,Lin Gui‑Zhi¹,Long Xiao‑Ling²,Xiao Xiao‑Min³,Song Yuan‑Zong¹

Affiliation:

1. Department of Pediatrics, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong 510630, P.R. China

2. Department of Pediatrics, Bo‑Ai Hospital of Zhongshan, Zhongshan, Guangdong 528400, P.R. China

3. Department of Gynecology and Obstetrics, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong 510630, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

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