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Answer:
60 per cent.
Explanation:
Generally in biological knowledge, people having hereditary pancreatitis disorder have mutations in the PRSS1 gene which result in inflammation of the pancreas possibly causing permanent tissue damage. This disorder is been inherited in an autosomal dominant fashion. Cation trypsinogen in a chain of enzymes made in the pancrease of human here aids food digestion. When found in an encoded situation, it shows more cationic trypsinogen.
First Plasmid is a chromosomal element often a circular DNA.
The uptake of a plasmid from the environment is NOT a common event reason being, bacteria naturally take up DNA from their environment in a process called transformation. Thus if a bacterium takes up a piece of DNA that cannot be maintained in a cell then that cell will not survive.
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