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Enhanced inactivation increases the sensitivity of pathogenic Cav1.3 L-type Ca2+-channel variants to dihydropyridine Ca2+ channel blockers

Termin

Datum:
Zeit:
Redezeit:
Diskussionszeit:
Ort / Stream:
H3

Session

Ion channels, drug development

Themen

  • CNS / endocrine pharmacology
  • Ion channels and membrane transporters

Mitwirkende

Ferenc Török (Innsbruck / AT), Nadine J Ortner (Innsbruck / AT), Jörg Striessnig (Innsbruck / AT)

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