Abstract
Ten inborn errors of metabolism are described in this chapter. Four of them, hyperlysinaemia/saccharopinuria, hydroxylysinuria, 2-amino-/2-oxoadipic aciduria, and glutaric aciduria type III, may be devoid of clinical significance, but some patients are retarded and show variable neurological abnormalities.
Cite
CITATION STYLE
APA
Hoffmann, G. F., & Kolker, S. (2012). Cerebral organic acid disorders and other disorders of lysine catabolism. In Inborn Metabolic Diseases: Diagnosis and Treatment (pp. 333–347). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-15720-2_23
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free