Associated Papers
The APOA1 p.Leu202Arg variant potentially causes autosomal recessive cardiac amyloidosis.
Yagi S et al.
Human Genome Variation, 2024
Apolipoprotein genetic variants and hereditary amyloidosis.
Jeraj N et al.
Current Opinion in Lipidology, 2021
Inborn errors of apolipoprotein A-I metabolism: implications for disease, research and development.
Zanoni P et al.
Current Opinion in Lipidology, 2020
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.
Dasari S et al.
Journal of Proteome Research, 2014
24650283 (PubMed )
Supplement: pr4011475_si_001.pdf
Mutation mapping of apolipoprotein A-I structure assisted with the putative cholesterol recognition regions.
Dergunov AD
Biochimica Et Biophysica Acta, 2013
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