Related Experiment Video
Updated: Oct 29, 2026

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Molecular basis of Refsum disease: identification of new mutations in the phytanoyl-CoA hydroxylase cDNA
G A Jansen1, S Ferdinandusse, O H Skjeldal
1University of Amsterdam, Academic Medical Center, Department of Clinical Chemistry, The Netherlands.
Journal of Inherited Metabolic Disease
|August 1, 1998
Abstract
No abstract available in PubMed .
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