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pro vyhledávání: '"Marwa ALMahroos"'
Autor:
Marwa ALMahroos, Mohammed AlMannai
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 5, Iss 1, Pp 17-19 (2022)
Background: Hereditary tyrosinemia type 1 (HT1) is an autosomal recessive inherited metabolic disorder caused by the fumerylacetoacetate hydrolase enzyme deficiency. It is characterized by liver dysfunction and/ or failure, renal tubular dysfunction.
Externí odkaz:
https://doaj.org/article/16f2cfe38b6e47aeaf0341ec4eb393a8