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Published in 2019 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms20102497
Abstract: Recessively-inherited NR2E3 gene mutations cause an unusual retinopathy with abnormally-increased short-wavelength sensitive cone (S-cone) function, in addition to reduced rod and long/middle-wavelength sensitive cone (L/M-cone) function. Progress toward clinical trials to treat patients with this…
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Keywords:
sensitive cone;
short wavelength;
cone cone;
wavelength sensitive ... See more keywords