Answer:
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Answer:
He should get his mitochondrial haplotype sequenced, given the genetic variation in mitochondrial sequences compared to Y chromosomes.
Explanation:
- Mitochondrial DNA haplotypes are specific regions of mitochondrial DNA that cluster with other mitochondrial sequences to show the phylogenetic origins of maternal lineages.
- Mitochondrial DNA haplotypes are associated with a range of phenotypes and disease.
- Mitochondrial DNA contains 37 genes, all of which are essential for normal mitochondrial function.
- Thirteen of these genes provide instructions for making enzymes involved in oxidative phosphorylation.
Answer:Tay-Sachs is an autosomal recessive disease caused by mutations in both alleles of a gene (HEXA) on chromosome 15. HEXA codes for the alpha subunit of the enzyme β-hexosaminidase A. This enzyme is found in lysosomes, organelles that break down large molecules for recycling by the cell.
Explanation:
Gravitational potential energy