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Article

A genetic defect in carnitine transport causing primary carnitine deficiency.

Progress in clinical and biological research - 1 Jan 1990

Stanley C A, Treem W R, Hale D E, Coates P M

Abstract excerpt

No abstract is available from the source.

Topics

Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenase, Long-Chain
Biological Transport
Cardiomyopathy, Hypertrophic
Carnitine
Cells, Cultured
Child
Child, Preschool
Fatty Acid Desaturases
Fibroblasts
Humans
Hyperglycemia
Infant
Kinetics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mutation

Source

Identifiers

PMID: 2326306

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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