Related Experiment Videos

Hepatic phosphorylase b kinase deficiency with normal enzyme activity in leukocytes and erythrocytes

H D Bakker¹, J A Taminiau, J E van den Berg

¹Emma Kinderziekenhuis, Division of Paediatrics, Academic Medical Centre, Amsterdam, The Netherlands.

Journal of Inherited Metabolic Disease

|January 1, 1991

Abstract

No abstract available in PubMed .

Related Concept Videos

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

Recommendations for pharmacological clinical trials in children with irritable bowel syndrome: the Rome foundation pediatric subcommittee on clinical trials.

Neurogastroenterology and motility·2016

Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy.

JIMD reports·2015

A survey of natural protein intake in Dutch phenylketonuria patients: insight into estimation or measurement of dietary intake.

Journal of the American Dietetic Association·2008

Review article: The clinical importance of growth in children with inflammatory bowel disease: is it important to the gastroenterologist?

Alimentary pharmacology & therapeutics·2008

A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria.

Human mutation·2006

Essential polyunsaturated fatty acids in plasma and erythrocytes of children with inborn errors of amino acid metabolism.

Molecular genetics and metabolism·2006

See all related articles