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. |
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Zdroj: | Journal of Pediatric Gastroenterology & Nutrition; 2022 Supplement, Vol. 74, p652-653, 2p |
Databáze: | Complementary Index |
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