Zobrazeno 1 - 1
of 1
pro vyhledávání: '"M. O. Amiryan"'
Publikováno v:
Nephrology (Saint-Petersburg). 27:18-30
This review presents the latest data on the classification, pathogenesis, clinical and genetic features, and therapy of primary hyperoxaluria types I, II, and III in children with autosomal recessive inheritance. ORPHA portal of orphan diseases prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3095a87ddb42353145fc213ce32c73bf
https://doi.org/10.36485/1561-6274-2023-27-1-18-30
https://doi.org/10.36485/1561-6274-2023-27-1-18-30
