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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2005 | 1 |
2017 | 1 |
2018 | 1 |
2024 | 0 |
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Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study.
Atheroscler Suppl. 2017 Oct;29:17-24. doi: 10.1016/j.atherosclerosissup.2017.07.002.
Atheroscler Suppl. 2017.
PMID: 28965616
Free article.
Autosomal dominant hypercholesterolemia in Catalonia: Correspondence between clinical-biochemical and genetic diagnostics in 967 patients studied in a multicenter clinical setting.
Martín-Campos JM, Plana N, Figueras R, Ibarretxe D, Caixàs A, Esteve E, Pérez A, Bueno M, Mauri M, Roig R, Martínez S, Pintó X, Masana L, Julve J, Blanco-Vaca F; Xarxa d’Unitats de Lípids i Arteriosclerosi (XULA).
Martín-Campos JM, et al.
J Clin Lipidol. 2018 Nov-Dec;12(6):1452-1462. doi: 10.1016/j.jacl.2018.09.002. Epub 2018 Sep 7.
J Clin Lipidol. 2018.
PMID: 30293936
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Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rate.
Graham CA, McIlhatton BP, Kirk CW, Beattie ED, Lyttle K, Hart P, Neely RD, Young IS, Nicholls DP.
Graham CA, et al.
Atherosclerosis. 2005 Oct;182(2):331-40. doi: 10.1016/j.atherosclerosis.2005.02.016.
Atherosclerosis. 2005.
PMID: 16159606
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