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. 2018 Oct 31;7:141. doi: 10.4103/abr.abr_80_18

Figure 3.

Figure 3

Sequence electropherogram of MYH15: c.C5557T (P.R1853C) variant. As one of the healthy individuals is homozygous for mutant allele and other affected individuals do not have homozygous mutant allele, this variant cannot be molecular etiology of the disease