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. 2017 Mar 15;25(6):783–787. doi: 10.1038/ejhg.2017.22

Figure 3.

Figure 3

The DNA sequence of a segment flanking p.(Tyr396*), c.1188 T>G in SLC22A5 is shown. Both parents and the unaffected brother are heterozygous variant carriers. The patient carries the variant in the homozygous state. The single base-pair substitution leads to a premature stop codon at amino-acid residue 396 of OCTN2.