How “Pharmacoresistant” is Cav2.3, the Major Component of Voltage-Gated R-type Ca2+ Channels?

Author:

Schneider Toni,Dibué Maxine,Hescheler Jürgen

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

Reference156 articles.

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4. Molecular analysis and functional expression of the human type E α1 subunit;Schneider;Receptors Channels,1994

5. Molecular Physiology of Low-Voltage-Activated T-type Calcium Channels;Perez-Reyes;Physiol Rev.,2003

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