Answer:
Women who carry one copy of the mutated gene still have normal color vision because they have another copy, which is not mutated, in the other X chromosome that will be the dominant one. As a result, the women are carriers of the mutated gene but not color blind.
Explanation:
Colorblindness is a sex-linked mutation. A woman has two X chromosomes, while a man has one X chromosome and one Y chromosome. The mutated gene that causes color blindness is on the X chromosome, and it is OPN1LW. So if a woman has one mutated OPN1LW in one of her two X chromosomes, the OPN1LW gene in the other X chromosome will be the dominant one stopping the woman from being colorblind.
In the case of men, as they only have one X chromosome, if there is a mutation on the OPN1LW in the X chromosome, the men will be colorblind because there is no extra copy of the gene, as it is in women.
Answer:
Rods
Explanation:
Rods are specialized photoreceptors that function best in low-light conditions. They are a major part of our vision in dimly lit environments, as well as our perception of movement in our peripheral vision.
The longest phase of mitosis is prophase. Because the nuclear membrane disappears, Nucleolus disintegrates, and the DNA condensed to form chromosomes (each chromosome is composed of sister chromatids attached around centromere.)
B is correct the births exceed deaths
