In a cross,one parent has a mutation in its mitochondria. In this case,this parent is taken as the male. During analysis,in which offspring is this mutation observed in the $F_2$ generation?

  • A
    In $\frac{1}{3}$ of the offspring
  • B
    Not observed in any offspring
  • C
    In all offspring
  • D
    In $50\%$ of the offspring

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