Wei‐Xia Lin

SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China

Yuan‐Zong Song, Zhan‐Hui Zhang, Wei‐Xia Lin et al. · PLoS ONE · 2013 · 62 citations · Full text

Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution

Wei‐Xia Lin, Han-Shi Zeng, Zhan‐Hui Zhang et al. · Scientific Reports · 2016 · 54 citations · Full text

Genetics, Genetic Epidemiology, Diagnosis +21

Sodium taurocholate cotransporting polypeptide (NTCP) deficiency: Identification of a novel <i>SLC10A1</i> mutation in two unrelated infants presenting with neonatal indirect hyperbilirubinemia and remarkable hypercholanemia

Jian‐Wu Qiu, Mei Deng, Ying Cheng et al. · Oncotarget · 2017 · 35 citations · Full text

Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for citrin deficiency

Zhan‐Hui Zhang, Wei‐Xia Lin, Mei Deng et al. · Gene · 2012 · 24 citations

Autoimmune Disease, Medicine, Genetics +11

Clinical, Molecular and Functional Investigation on an Infant with Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency (NICCD)

Zhan‐Hui Zhang, Wei‐Xia Lin, Mei Deng et al. · PLoS ONE · 2014 · 18 citations · Full text