Fig. 2
From: Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl
The results of direct sequencing by Sanger. The Fragment of exon 9 of the IDS gene: a) the proband: deletion p.1436_1440 AGCCG in the “homozygous” state; b) normal sequence according to reference NM_000202.5; c) the father: a normal variant of the sequence of the IDS gene; d) the mother: deletion p.1436_1440 AGCCG in the heterozygous state