Genetic contribution of ABCC2 to Dubin‐Johnson syndrome and inherited cholestatic disorders-Reference-Cited by-同舟云学术

Genetic contribution of ABCC2 to Dubin‐Johnson syndrome and inherited cholestatic disorders

Published:2019-10-13 Issue:1 Volume:40 Page:163-174
ISSN:1478-3223
Container-title:Liver International
language:en
Short-container-title:Liver Int

Author:

Corpechot Christophe¹²,Barbu Véronique²³,Chazouillères Olivier¹²,Broué Pierre⁴,Girard Muriel⁵⁶,Roquelaure Bertrand⁷,Chrétien Yves¹,Dong Catherine¹,Lascols Olivier²³,Housset Chantal¹²,Jéru Isabelle²³^ORCID

Affiliation:

1. Centre de Référence des Maladies Inflammatoires des Voies Biliaires et des Hépatites Auto‐Immunes (MIVB‐H) Filière de Santé des Maladies Rares du Foie de l'enfant et de l'adulte (FILFOIE) Assistance Publique‐Hôpitaux de Paris Hôpital Saint‐Antoine Paris France

2. INSERM Centre de Recherche Saint‐Antoine (CRSA) Institut Hospitalo‐Universitaire de Cardio‐métabolisme et Nutrition (ICAN) Sorbonne Université Paris France

3. Laboratoire Commun de Biologie et Génétique Moléculaires Assistance Publique‐Hôpitaux de Paris Hôpital Saint‐Antoine Paris France

4. Centres de compétences maladies rares du foie de l'enfant et Centre de référence constitutif maladies héréditaires du métabolisme Hépatologie Pédiatrique et Maladies Héréditaires du Métabolisme Hôpitaux de Toulouse Hôpital des Enfants Toulouse France

5. Service d'Hépato‐Gastroentérologie et Nutrition Pédiatrique Assistance Publique‐Hôpitaux de Paris Hôpital Necker Enfants‐Malades Paris France

6. INSERM U1151 Institut Necker Enfants‐Malades Université Paris Descartes Paris France

7. Service d'Hépato‐Gastroentérologie et Nutrition Pédiatrique Assistance Publique‐Hôpitaux de Marseille Hôpital de la Timone Enfants Marseille France

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/liv.14260

Reference49 articles.

1. CHRONIC IDIOPATHIC JAUNDICE WITH UNIDENTIFIED PIGMENT IN LIVER CELLS

2. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome

3. Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome

4. Genomic Structure of the Canalicular Multispecific Organic Anion–Transporter Gene (MRP2/cMOAT) and Mutations in the ATP-Binding–Cassette Region in Dubin-Johnson Syndrome

5. Physiological, pharmacological and clinical features of the multidrug resistance protein 2

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