Insulin stimulated upregulation of OCTN2 carnitine transporters is impaired in patients with Primary carnitine deficiency
Dahl R; Sjúrðarson T; Paturson P; Ingersen A; Andersen PF; Jørgensen JEM; Simpson EJ; Rasmussen J · 2025 · Preprint
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
Background Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of functional carnitine transporters OCTN2 (Organic Cation/Carnitine Transporter 2), which has been linked to several cases of sudden…
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Metadata source: Europe PMC · DOI 10.1101/2025.09.22.677318