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. 2015 Mar 23;11(3):e1005059. doi: 10.1371/journal.pgen.1005059

Fig 3. Characterization of ADAMTS20 mutation in NSDTRs.

Fig 3

A. Chromatograms of ADAMTS20 cDNA sequence from embryo control and NSDTR case depicting the AA deletion and predicted premature stop codon. * denotes the deleted nucleotides in the 13 NSDTR cases. B. Schematic functional domain organization of ADAMTS20. SP- signal peptide TS- Thrombospondin type 1 motif[26]. bt Bei1—reflects the location of point mutation responsible for the bt Bei1allele.