In humans, the recessive allele that causes a form of red-green colour blindness (c) is found on the X chromosome. a.) Determine the genotypes and phenotypes of the F1 generation from a colour-blind father and a mother who is homozygous for normal colour vision. b.) Determine the genotypes and phenotypes of the F1 generation from a father who has normal colour vision and a mother who is heterozygous for colour vision. c.) Draw a Punnett square to determine the genotypes of parents that could produce a daughter who is colour-blind

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Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.