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Peloquin, J.; Rehak, R.; Doering, C.; McRory, J. (2007). "Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W". Neuroscience. 150 (2): 335–345. doi:10.1016/j.neuroscience.2007.09.021. PMID 17949918. 

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