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Fig. 2 | Pediatric Rheumatology

Fig. 2

From: A case report of a novel compound heterozygous mutation in a Brazilian patient with deficiency of Interleukin-1 receptor antagonist (DIRA)

Fig. 2

DNA sequence electropherograms demonstrating the p.Ile71_Pro75del and p.Gln45Ter heterozygous mutations in IL1RN. Sanger sequencing results for IL1RN mutations in DIRA patient. Electropherograms of the two mutations are reported. a p.Ile71_Pro75del, reverse strand and (b) p.Gln45Ter, forward strand. Black arrows indicated (A) the first and last nucleotides of the deletion; b the nucleotide mutated

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Pediatric Rheumatology

ISSN: 1546-0096