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. 2021 Jan 1;56(1):68–71. doi: 10.14744/TurkPediatriArs.2020.37880

Figure 1.

Figure 1

Pedigree of the family carrying POMT2 mutation related LGMD2N and sequence analysis of POMT2 revealed a homozygous missense mutation of c.1261C>T (p.Arg421Trp)(R421W) in exon 12