A syndrome of hereditary tyrosinemia in mink (Mustela vison Schreb.).

摘要: A hereditary disease in mink (Mustela vison Schreb.) leading to death when the affected kits are about six weeks old has been investigated. The disorder is inherited as a simple autosomal recessive character. Strongly elevated plasma tyrosine concentration an outstanding feature of disease. An enzyme defect aminotransferase (EC 2.6.1.5) or 4-hydroxyphenylpyruvate dioxygenase 1.13.11.27) considered together with possibility parallel between and tyrosinosis tyrosinemia man.