Respuesta :
The type of mutation that causes this translation error is called deletion. Deletion occurs when a section of a DNA is deleted or lost. In cystic fibrosis, three nucleotides are deleted that results in the lost of phenylalanine.
The type of mutation that causes this translation error in cystic fibrosis is
called deletion.
What is Deletion?
Deletion occurs as a result of a segment of the DNA being left during the
process of replication.
In the case of cystic fibrosis, the section of the DNA lost contains the
three nucleotides which codes for phenylalanine. This thereby results in
the loss of this amino acid and in the formation of the genetic disorder.
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