Related references
Note: Only part of the references are listed.Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders
Christophe Corpechot et al.
LIVER INTERNATIONAL (2020)
A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China
Lina Wu et al.
ORPHANET JOURNAL OF RARE DISEASES (2020)
Mutation spectrum and biochemical features in infants with neonatal Dubin-Johnson syndrome
Kwang Yeon Kim et al.
BMC PEDIATRICS (2020)
Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin-Johnson syndrome in a Chinese gril: A case report
Yuan Li et al.
WORLD JOURNAL OF CLINICAL CASES (2019)
Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan
Takao Togawa et al.
JOURNAL OF PEDIATRICS (2018)
Inherited disorders of bilirubin clearance
Naureen Memon et al.
PEDIATRIC RESEARCH (2016)
Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing
Takao Togawa et al.
JOURNAL OF PEDIATRICS (2016)
Neonatal Dubin-Johnson syndrome: Novel compound heterozygous mutation in the ABCC2 gene
Hitoshi Okada et al.
PEDIATRICS INTERNATIONAL (2014)
Ontogeny of Human Hepatic and Intestinal Transporter Gene Expression during Childhood: Age Matters
Miriam G. Mooij et al.
DRUG METABOLISM AND DISPOSITION (2014)
Mutational analysis of ABCC2 gene in two siblings with neonatal-onset Dubin Johnson syndrome
L. Pacifico et al.
CLINICAL GENETICS (2010)
Neonatal Dubin-Johnson Syndrome: Long-term follow-up and MRP2 mutations study
JH Lee et al.
PEDIATRIC RESEARCH (2006)
Developmental expression of canalicular transporter genes in human liver
HL Chen et al.
JOURNAL OF HEPATOLOGY (2005)
Guideline for the evaluation of cholestatic jaundice in infants: Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition
V Moyer et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2004)
Radixin deficiency causes conjugated hyperbilirubinemia with loss of Mrp2 from bile canalicular membranes
S Kikuchi et al.
NATURE GENETICS (2002)
Share Paper
