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Biology, 26.07.2019 19:10 NewKidnewlessons

Aman has a mutation in a mitochondrial gene encoding a subunit of the atp synthase complex. the mutation leads to a defective atp synthase that is not able to synthesize atp effectively, and this in turn leads to extreme muscle weakness in the affected individual. the man's wife is phenotypically normal. they have two boys and two girls. what proportion of their children is expected to have the disease?

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