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Amino acid tyrosinemia type

Tyrosine derives from the breakdown of dietary or tissue proteins or through the hydroxylation of the essential amino acid phenylalanine. Hepatorenal tyrosinemia (tyrosinemia type I, TYR-I) is an autosomal recessive disease caused by a deficiency of the enzyme fumarylacetoacetase (Figure 55-7),... [Pg.2217]

Amino acids Amino acidopathies (PKU, tyrosinemia type I) Dried blood plasma, urine ESI-MS/MS [12]... [Pg.256]

See other pages where Amino acid tyrosinemia type is mentioned: [Pg.2218] [Pg.2218] [Pg.199] [Pg.25] [Pg.40] [Pg.42] [Pg.293] [Pg.294] [Pg.143] [Pg.143]

See also in sourсe #XX -- [ Pg.2217 , Pg.2218 , Pg.2218 , Pg.2219 ]

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Acidity, types

Acids types

Amino-acids types 144

Tyrosinemia