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Is Cav1.3 a feasible therapeutic target for a rare neurodevelopmental disorder?

Nadine J Ortner1

  • 1Department of Pharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.

Expert Opinion on Therapeutic Targets
|December 13, 2024
PubMed
Abstract

No abstract available in PubMed .

Keywords:
CACNA1DCa2+ channel blockersCav1.3 Ca2+ channelsde novo missense mutationsdihydropyridinesneurodevelopmental disease

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