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. 2015 Nov 25;10(11):e0143915. doi: 10.1371/journal.pone.0143915

Fig 6. ApoA-I structure model.

Fig 6

Location of mutations (yellow) in the vicinity of the A164S variant (red) that are linked to hereditary amyloidosis, or associated with LCAT deficiency and low HDL levels, are depicted in the lipid-free structure model [52].