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Tyrosinemia Type III: A Case Report with a Seven Years Follow-up
Tyrosinemia Type III: A Case Report with a Seven Years Follow-up

Saba Vakili; Mohammadreza Emami; Moein Mobini; Rahim Vakili

Volume 9, Issue 6 , June 2021, , Pages 13853-13857

https://doi.org/10.22038/ijp.2021.56791.4451

Abstract
  Hereditary tyrosinemia type III (OMIM 276710) is a rare inborn error of tyrosine metabolism caused by the deficiency of 4-hydroxyphenylpyruvate dioxygenase (HPD). This ...  Read More