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Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis.
Mol Genet Genomic Med. 2019 Dec;7(12):e1007. doi: 10.1002/mgg3.1007. Epub 2019 Oct 16.
Mol Genet Genomic Med. 2019.
PMID: 31617323
Free PMC article.
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia.
Dong W, Wong KHY, Liu Y, Levy-Sakin M, Hung WC, Li M, Li B, Jin SC, Choi J, Lopez-Giraldez F, Vaka D, Poon A, Chu C, Lao R, Balamir M, Movsesyan I, Malloy MJ, Zhao H, Kwok PY, Kane JP, Lifton RP, Pullinger CR.
Dong W, et al. Among authors: balamir m.
J Lipid Res. 2022 Jun;63(6):100209. doi: 10.1016/j.jlr.2022.100209. Epub 2022 Apr 20.
J Lipid Res. 2022.
PMID: 35460704
Free PMC article.
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