This mutation, at first glance could be considered a dominant mutation as there are many affected individuals and it mostly did not skip a generation. However, it can be seen at the left side that it stopped in the 2nd generation father.
The pedigree shown below is typical of :
A. An autosomal dominant mutation.
B. An autosomal recessive mutation
C. An X-linked mutation
D. A mitochondrial mutation
E. None of the answers listed above are correct.
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