Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathy-Reference-Cited by-同舟云学术

Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathy

Published:2017-09-12 Issue:2 Volume:38 Page:358-364
ISSN:1478-3223
Container-title:Liver International
language:en
Short-container-title:Liver Int

Author:

Besmond Claude¹,Valla Dominique²,Hubert Laurence¹,Poirier Karine¹,Grosse Brigitte³,Guettier Catherine⁴,Bernard Olivier⁵,Gonzales Emmanuel³⁵,Jacquemin Emmanuel³⁵^ORCID

Affiliation:

1. Inserm U1163; Imagine Institute for Genetic Diseases; Necker University Hospital; Paris France

2. Hepatology Unit; National Reference Centre for Rare Vascular Liver Diseases; Beaujon Universitary Hospital, Unity; Clichy France

3. Inserm; UMR-S1174; Hepatinov; University of Paris-Sud 11; Orsay France

4. Pathology Unit; Hepatinov; Bicêtre Universitary Hospital; Assistance Publique-Hôpitaux de Paris; University of Paris-Sud; Le Kremlin Bicêtre France

5. Pediatric Hepatology and Pediatric Liver Transplantation Unit; National Reference Centre for Rare Pediatric Liver Diseases; Hepatinov; Bicêtre Universitary Hospital; Assistance Publique-Hôpitaux de Paris; University of Paris-Sud; Le Kremlin Bicêtre France

Funder

AMFE (“Association Maladies Foie Enfants”, Malakoff, France)

MLD (Monaco Liver Disorder, Monaco)

Foundation Rumsey-Cartier (Geneva, Switzerland)

Imagine institute for Genetic Diseases (Paris, France)

Publisher

Wiley

Subject

Hepatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/liv.13547/fullpdf

Reference11 articles.