Fig. 1From: A very early diagnosis of Alstrӧm syndrome by next generation sequencingSequence chromatograms of the variants identified in the proband. The chromatograms show the c.1196_1202del: p.(Thr399Lysfs*11) (upper panel) and the c.11310_11313del: p.(Glu3771Trpfs*18) (lower panel) heterozygous deletions. The family pedigree shows the compound heterozygous state of these two variants in the probandBack to article page