TAT Polyclonal Antibody, 20ul Aspirating Pipets ranging from neonatal adrenoleukodystrophy to
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TAT Polyclonal Antibody, 20ul Aspirating Pipets ranging from neonatal adrenoleukodystrophy toThis nuclear gene TAT (tyrosine aminotransferase) encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L tyrosine into p hydroxyphenylpyruvate. Mutations in TAT cause tyrosinemia (type II, Richner Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X linked.
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