Related Experiment Videos

Comment on the diagnosis of inborn errors of metabolism in Australia

Australian Paediatric Journal

|June 1, 1976

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Failure to confirm abnormal copper utilization in crinkler (cr) mice.

Biological trace element research·2013

Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.

Molecular genetics and metabolism·2000

Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobe.

Journal of inorganic biochemistry·1998

Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.

Human molecular genetics·1998

Early treatment of Menkes disease with parenteral copper-histidine: long-term follow-up of four treated patients.

American journal of medical genetics·1998

DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.

Human mutation·1997

See all related articles