Assume that a particular genetic condition in a mammalian species causes an inability to digest starch This disorder occurs with equal frequency in males and females in most cases neither parent is af?

Answer 1

It is an autosomal recessive trait. it cant be sex-linked because it would show up in males more than females.

Answer 2

This genetic condition is likely an autosomal recessive trait since it occurs with equal frequency in males and females. If neither parent is affected, it suggests that both parents are carriers of the condition. In order for a child to be affected, they would need to inherit two copies of the recessive allele, one from each carrier parent.