lbinism is an autosomal recessive condition where little or no melanin pigment is produced. A woman (call her W) had an affected brother (B). This woman's daughter (M) is planning to have a child. The intended father (F) in this mating had a sister (S) who has albinism. a. Draw the pedigree of the family. Use defined symbols to indicate genotypes.

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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.