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[In 16 ESCS patients with the most common NR2E3 mutation, R311Q, we documented an abnormal ratio of S to L/M cone function and progressive retinal degeneration/studied the postmortem retina of an ESCS patient homozygous for NR2E3 R311Q]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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