Phenotypic spectrum and diagnostic pitfalls of ABCB4 deficiency depending on age of onset-Reference-Cited by-同舟云学术

Phenotypic spectrum and diagnostic pitfalls of ABCB4 deficiency depending on age of onset

Published:2018-03-22 Issue:5 Volume:2 Page:504-514
ISSN:2471-254X
Container-title:Hepatology Communications
language:en
Short-container-title:Hepatology Communications

Author:

Schatz Stephanie Barbara¹,Jüngst Christoph²,Keitel‐Anselmo Verena³,Kubitz Ralf³,Becker Christina²,Gerner Patrick⁴,Pfister Eva‐Doreen¹,Goldschmidt Imeke¹,Junge Norman¹,Wenning Daniel⁵,Gehring Stephan⁶,Arens Stefan⁷,Bretschneider Dirk⁸,Grothues Dirk⁹,Engelmann Guido¹⁰,Lammert Frank²,Baumann Ulrich¹¹¹

Affiliation:

1. Hannover Medical School, Division of Pediatric Gastroenterology and Hepatology, Department of Pediatric Kidney, Liver, and Metabolic DiseasesHannover Germany

2. Department of Medicine IISaarland University Medical CenterHomburg Germany

3. University Hospital, Heinrich Heine University Düsseldorf, Department of Gastroenterology, Hepatology and Infectious DiseasesDüsseldorf Germany

4. Division of Pediatric Gastroenterology, Clinic for Pediatrics IIUniversity Hospital, University EssenEssen Germany

5. Department of General PediatricsUniversity HospitalHeidelberg Germany

6. Department of PediatricsUniversity Medical Center of the Johannes Gutenberg University MainzMainz Germany

7. Klinikum KasselPediatric GastroenterologyKassel Germany

8. Klinik St. MarienstiftMagdeburg Germany

9. KUNO University Children's HospitalRegensburg Germany

10. LukaskrankenhausChildren's HospitalNeuss Germany

11. Institute of Immunology and ImmunotherapyUniversity of BirminghamBirmingham United Kingdom

Funder

Billy Rubin

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep4.1149

Reference44 articles.

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2. Mutations in TJP2 cause progressive cholestatic liver disease

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4. Progressive Familial Intrahepatic Cholestasis with High γ-Glutamyltranspeptidase Levels in Taiwanese Infants: Role of MDR3 Gene Defect?

5. ABCB4 Heterozygous Gene Mutations Associated With Fibrosing Cholestatic Liver Disease in Adults

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