The Korean Journal of Blood Transfusion : eISSN 2383-6881 / pISSN 1226-9336

Fig. 1.

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Fig. 1.

Genotyping results of the case. The patient showed an intact RHD gene (left) with two single nucleotide changes from the reference sequence NM_016124. c.711delC (middle) was identified to be the causative variant, while c.1154-31 C>T (right) is a frequently observed polymorphism in Caucasians.

Korean J Blood Transfus 2019;30:168-73
© 2019 Korean J Blood Transfus