Answer: in humans most come from the cytoplasm of the ovum or egg cell
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how are mitochondria inherited?
Mitochondrial diseases are a group of disorders caused by dysfunctional mitochondria the organelles that generate energy for the cell. Mitochondria are found in every cell of the human body except red blood cells and convert the energy of food molecules into the ATP that powers most cell functions.
Mitochondrial Diseases - RightDiagnosis.com
Mitochondrion - Wikipedia
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Wed Dec 12 2018 · See additional information. Mitochondrial inheritance: The inheritance of a trait encoded in the mitochondrial genome . Because of the oddities of mitochondria mitochondrial inheritance does not obey the classic rules of genetics. Persons with a mitochondrial disease may be male or female but they are always related in the maternal line and no male with the disease can transmit it to his children.
Because mitochondrial diseases(diseases due to malfunction of mitochondria) can be inherited both maternally and through chromosomal inheritance the way in which they are passed on from generation to generation can vary greatly depending on the disease. Mitochondrial genetic mutations that occur in the nuclear DNA can occur in any of the chromosomes (depending on the species). Mutations inherited through the chromosomes can be autosomal dominant or recessive and can also be sex-linked domina…
Mon Nov 18 2019 · Unlike the nuclear DNA that is inherited from both parents mitochondrial DNA is inherited from the mother . Each mitochondrion carries two to ten copies of the mitoch...
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