Displaying items by tag: department of optometry and vision science
A modifier gene is one that changes the observable characteristics, called the phenotype, or molecular expression of other genes.
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The model may provide novel insights into RP59 disease mechanism that will guide future testing of therapeutic interventions.
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UAB experts advise parents to think about keeping kids safe this Halloween.
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Results show that retinitis pigmentosa 59 may not be a congenital disorder of glycosylation, as was long assumed.
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Optometrists can identify potential vision problems in infants as early as 6 to 12 months.
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