| Authors: |
Almes M; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France., Gardin A; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France., Davit-Spraul A; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France.; Biochemistry Unit., Bouligand J; Molecular Genetics and Pharmacogenetics, Bicêtre Hospital, Assistance Publique - Hôpitaux de Paris, University Paris-Saclay, Le Kremlin-Bicêtre, France., Habes D; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France., Jacquemin E; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France. |
