bibliographic resource 1046152 [br/1046152]
https://w3id.org/oc/corpus/br/1046152
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- Congenital Stationary Night Blindness Type 2 Mutations S229P, G369D, L1068P, and W1440X Alter Channel Gating or Functional Expression of Cav1.4 L-type Ca2+ Channels
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