[Glutaric aciduria type I with a low-excretion biochemical phenotype associated to a new mutation]

Rev Neurol. 2007 Jul;45(2):127-8.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Amino Acid Metabolism, Inborn Errors* / genetics
  • Amino Acid Metabolism, Inborn Errors* / physiopathology
  • Female
  • Glutarates / urine*
  • Humans
  • Mutation
  • Phenotype

Substances

  • Glutarates
  • glutaric acid