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pro vyhledávání: '"Leila, Ben Othmene"'
Autor:
Imene, Braham, Bassem, Charfeddine, Leila, Ben Othmene, Souhir, Neffati, Aida, Mtar, Jihene, Ben Abdallah, Med, Ali Smach, Hedi, Dridi, Khalifa, Limem
Publikováno v:
Annales de biologie clinique. 70(1)
Congenital galactosemia is a hereditary, autosomal recessive and metabolic disease. It is linked to an enzyme deficiency, more commonly known by the deficiency of galactose-1- phosphate uridyltransferase (GALT), which is responsible for an accumulati