Defects in Amino Acid Metabolism
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Phenylketonuria
Type I Tyrosinemia
-Tyrosinosis
Type II Tyrosinnemia
-Richner-Hanhart Syndrome
Type III Tyrosinemia
Alkaptonuria
Homocystinuria
Histidinemia
Maple Syrup Urine Disease, MSUD
Methylmalonic Aciduria
Glycine encephalopathy, GCE
- Non-ketotic hyperglycinemia, NKH
Hyperlysinemia
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Michael W. King, Ph.D / IU School of Medicine / miking at iupui.edu
Last modified: June 11, 2009