US EPA

7491424 

Journal Article 

Inborn errors of metabolism: Part 2: Specific disorders 

Levy, PA 

2009 

1 

Pediatrics in Review
ISSN: 0191-9601
EISSN: 1526-3347 

30 

4 

e22-e28 

English 

10.1542/pir.30-4-e22 

carbamate kinase; fructose bisphosphatase; glutamate acetyltransferase; oligosaccharide; acidosis; amino acid metabolism; chondrodysplasia punctata; disorders of mitochondrial functions; disorders of peroxisomal functions; galactosemia; glycogen storage disease; hereditary fructose intolerance; homocystinuria; human; inborn error of metabolism; lipidosis; lysosome storage disease; maple syrup urine disease; mucopolysaccharidosis; newborn screening; nucleotide sequence; phenylketonuria; protein glycosylation; short survey; tyrosinemia; urea cycle; urinalysis; Zellweger syndrome; article; child; classification; inborn error of metabolism; infant; newborn; preschool child; Child; Child, Preschool; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Neonatal Screening