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Additional file 1 of The LDLR c.501C>A is a disease-causing variant in familial hypercholesterolemia
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posted on 2021-09-13, 03:10 authored by Haochang Hu, Ruoyu Chen, Yingchu Hu, Jian Wang, Shaoyi Lin, Xiaomin ChenAdditional file 1: Supplement Figure 1. Target sequences on LDLR by Sanger sequencing. The top row of the sequence represented the original sequence, and the second row showed the mutant sequence. And the framed base indicated the mutation (LDLR c.501C>A).
