They wouldn't be able to see the right color
Answer:
The correct answers are "heterozygous", and "homozygous dominant".
Explanation:
Galactosemia is a condition where people are not able to process the sugar galactose. People with this condition have one gene mutated, which does not allow the proper synthesis of the enzyme that breaks down galactose. Galactosemia is inherited as an autosomal recessive genetic condition, therefore, only children that are homozygous recessive develop the condition. Children that are heterozygous or homozygous dominant, will not develop galactosemia.
The gene responsible for lactose persistence among adults in Europe is a regulatory gene.
The cell would die. This is because mitochondria are essential for making energy that the cell can use, if the mitochondria stopped working this energy would not longer be available to the cell. If the cell does not have energy, it cannot perform vital functions like respiration.
