Respuesta :
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.
