Zobrazeno 1 - 1
of 1
pro vyhledávání: '"S Samanpour"'
Publikováno v:
Armaghane Danesh Bimonthly Journal, Vol 24, Iss 5, Pp 820-829 (2019)
Background & aim: Tyrosinemia is a recessive autosomal genetic disease due to the defect of fumaril acetoacetate hydrolase (FAH). About 40 pathogenic mutations have been reported for this gene. The aim of the present study was to determine and design
Externí odkaz:
https://doaj.org/article/b25b4717e1bd4b6892eba3a953918e86
