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Impact of MCT1 Haploinsufficiency on the Mouse Retina

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Retinal Degenerative Diseases

Abstract

The monocarboxylate transporter 1 (MCT1) is highly expressed in the outer retina, suggesting that it plays a critical role in photoreceptors. We examined MCT1 +/− heterozygotes, which express half of the normal complement of MCT1. The MCT1 +/− retina developed normally and retained normal function, indicating that MCT1 is expressed at sufficient levels to support outer retinal metabolism.

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Acknowledgments

This work was supported by grants from NIH (R01EY12042) and Department of Veterans Affairs (I01BX2340) and by the Foundation Fighting Blindness and Research to Prevent Blindness.

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Correspondence to Neal S. Peachey .

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Peachey, N.S. et al. (2018). Impact of MCT1 Haploinsufficiency on the Mouse Retina. In: Ash, J., Anderson, R., LaVail, M., Bowes Rickman, C., Hollyfield, J., Grimm, C. (eds) Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology, vol 1074. Springer, Cham. https://doi.org/10.1007/978-3-319-75402-4_46

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