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pro vyhledávání: '"K. G. Van Wyk"'
Publikováno v:
Journal of Inherited Metabolic Disease. 23:677-683
Tyrosinaemia types I and II are caused by enzyme deficiencies in the tyrosine catabolism pathway. Successful treatment is possible with the novel enzyme inhibitor NTBC in tyrosinaemia type I and with dietary tyrosine and phenylalanine restriction in