Answer:
Missense
Explanation:
The key in this question is 'which type of mutation causes this problem.
The description of this disease gives the the answer. A replacement of a glutamic acid amino acid with and Valine amino acid is called missense.
Silent mutation do not cause any difference in structure or function of the protein.
Insertions are an additional nucleotide or 2 added to the sequence
Frameshifts are the same as insertions, but the insertion occurs in part of the gene that codes for the protein. Because of that 'insertion' the reading frame of this gene is out and the protein sequence is not correct.