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Article
Nature Neuroscience  5, 364 - 370 (2002)
Published online: 25 February 2002; | doi:10.1038/nn817

Reorganization of human cortical maps caused by inherited photoreceptor abnormalities

Heidi A. Baseler1, Alyssa A. Brewer2, Lindsay T. Sharpe3, Antony B. Morland1, Herbert Jägle3 & Brian A. Wandell1, 2

1  Department of Psychology, Stanford University, Stanford, California, USA

2  Neuroscience Program, Stanford University, Stanford, California, USA

3  University of Tübingen, Tübingen, Germany

Correspondence should be addressed to Brian A. Wandell wandell@stanford.edu
We describe a compelling demonstration of large-scale developmental reorganization in the human visual pathways. The developmental reorganization was observed in rod monochromats, a rare group of congenitally colorblind individuals who virtually lack cone photoreceptor function. Normal controls had a cortical region, spanning several square centimeters, that responded to signals initiated in the all-cone foveola but was inactive under rod viewing conditions; in rod monochromats this cortical region responded powerfully to rod-initiated signals. The measurements trace a causal pathway that begins with a genetic anomaly that directly influences sensory cells and ultimately results in a substantial central reorganization.

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Nature Neuroscience
ISSN: 1097-6256
EISSN: 1546-1726
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