fMRI and gene therapy in adults with CNGB3 mutation

fMRI and gene therapy in adults with CNGB3 mutation

Achromatopsia is an inherited retinal disease that affects 1 in 30,000–50,000 individuals and is characterised by an absence of functioning cone photoreceptors from birth. This results in severely reduced visual acuity, no colour vision, marked sensitivity to light and involuntary oscillations of th...

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Bibliographic Details
Main Authors: Elaine J. Anderson, Tessa M. Dekker, Mahtab Farahbakhsh, Nashila Hirji, D. Samuel Schwarzkopf, Michel Michaelides, Geraint Rees
Format: Article
Language:English
Published: Elsevier 2024-09-01
Series:Brain Research Bulletin
Subjects:
FMRI
Achromatopsia
Gene therapy
Visual cortex
Plasticity
Psychophysics
Online Access:http://www.sciencedirect.com/science/article/pii/S036192302400159X

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http://www.sciencedirect.com/science/article/pii/S036192302400159X

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