Journal of Rheumatic Diseases

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Fig. 4. Sanger sequencing of the mutations in allele c.2548C>T (p.Gln850*) (nonsense mutation) (A) and c.3051G>T (p.Trp1017Cys) (missense mutation) (B) (arrows).
J Rheum Dis 2021;28:101~106 https://doi.org/10.4078/jrd.2021.28.2.101
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