Biochemical studies on the enzymatic deficiencies in hereditary tyrosinemia
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference29 articles.
1. Tyrosinosis and tyrosinemia;Du Bn,1978
2. Tyrosinemia. An inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal tubular defects (de Toni-Debré-Fanconi syndrome);Gentz;J Pediatr,1965
3. Studies on tyrosinosis. 2. Activity of transaminase, para-hydroxyphenylpyruvate oxidase and homogentisic acid oxidase;Taniguchi;Br Med J,1965
4. Biochemical observations on socalled hereditary tyrosinemia;Gaull;Pediatr Res,1970
5. On the enzymic defects in hereditary tyrosinemia;Lindblad,1977
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