Journal
EUKARYOTIC CELL
Volume 5, Issue 8, Pages 1441-1445Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/EC.00160-06
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Mutations in the human HPD gene (encoding 4-hydroxyphenylpyruvic acid dioxygenase) cause hereditary tyrosinemia type 3 (HT3). We deleted the Aspergillus nidulans homologue (hpdA). We showed that the mutant strain is not able to grow in the presence of phenylalanine and that it accumulates increased concentrations of tyrosine and 4-hydroxyphenylpyruvic acid, mimicking the human HT3 phenotype.
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