Skip to main content
. 2017 Apr;22(2):131–133. doi: 10.17712/nsj.2017.2.20160468

Figure 1.

Figure 1

- Sequence analysis of the patient’s DNA shows a homozygous mutation. The part of sequence analysis is from part of exon 25, showing G>A change at 2963, resulting in Arg998Gln amino acid replacement. The parents are heterozygous for the same change.