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. 2013 Oct 3;2013:bcr2013200838. doi: 10.1136/bcr-2013-200838

FigureĀ 3.

FigureĀ 3

The patient carries a homozygous c.517A>G; Asn173Asp mutation in the SLC19A3 gene. Both parents carry the same mutation in heterozygous state, demonstrating that it segregates with the disease within the family pedigree. The control at the top shows a homozygous wild-type sequence.