Severe progressive intrahepatic cholestasis, secondary to homozygous mutation of TJP2; a single high volume pediatric liver transplant centre experience.

Autor: Kumar, K., Akhtar, A. S., Albogami, D., Binomar, H., Alhussaini, H., Almanea, H., Aldana, A., Broering, D., Shagrani, M.
Zdroj: Journal of Pediatric Gastroenterology & Nutrition; 2022 Supplement, Vol. 74, p652-653, 2p
Databáze: Complementary Index
Externí odkaz: