4. The couple shown by the pedigree shown below, have 2 children, 1 girl with the disease and 1 boy without the disease as shown. What is the mode of inheritance? (is the disease autosomai recessive, autosomal dominant, or X-linked recessive?) Explain why you think this. Fill in the genotypes to help you answer this.

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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.