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Fig. 1 | BMC Medical Genetics

Fig. 1

From: A new genetic variant of hereditary apolipoprotein A-I amyloidosis: a case-report followed by discussion of diagnostic challenges and therapeutic options

Fig. 1

Secondary structure of ApoAI, based on the UNIPROT database (https://www.uniprot.org/uniprot/P02647). Helix is depicted with bold blue letters and turn region with orange bold. The sites of identified mutations, as provided by http://www.amyloidosismutations.com/cdna-aapoai.html are shown with red boxes. The L60P mutation described in the manuscript is also shown in red characters

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