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Hawkinsinuria: A Dominantly Inherited Defect of Tyrosine Metabolism with Severe Effects in Infancy
Hawkinsinuria: A Dominantly Inherited Defect of Tyrosine Metabolism with Severe Effects in Infancy
1981
Bridget Wilcken
Judith Hammond
Neville J. Howard
Timothy Bohane
Charles Hocart
B. Halpern
Keywords:
Tyrosine Metabolism
Hawkinsinuria
Surgery
Diabetes mellitus
Endocrinology
Internal medicine
Medicine
Tyrosine
Cyclohexenes
Cyclohexanecarboxylic acid
Correction
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