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Color "blindness"
Color 'blindness' is more accurately described as a color vision deficiency. The most prevalent type is red-green color blindness, an X-linked inherited condition caused by the absence of cones that process medium-wavelength light. Because the responsible gene is on the X chromosome, and men have only one X chromosome, this deficiency is far more common in men than in women. Women possess two X chromosomes, which typically provides a functional gene if the other is mutated. This condition impairs the ability to distinguish between certain colors, especially reds and greens.

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A male is diagnosed with red-green color vision deficiency, a condition linked to a gene on the X chromosome. His mother has normal color vision. What is the most likely explanation for how he inherited the condition?
A specific type of inherited color vision deficiency, which makes it difficult to distinguish between red and green, is observed far more frequently in males than in females. Which statement best analyzes the genetic reason for this difference in prevalence?