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Year | Number of Results |
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2004 | 1 |
2010 | 1 |
2013 | 1 |
2017 | 1 |
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Genetic screening of patients with familial hypercholesterolaemia (FH): a New Zealand perspective.
Atheroscler Suppl. 2004 Dec;5(5):13-5. doi: 10.1016/j.atherosclerosissup.2004.09.001.
Atheroscler Suppl. 2004.
PMID: 15556094
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy.
Bertolini S, Pisciotta L, Rabacchi C, Cefalù AB, Noto D, Fasano T, Signori A, Fresa R, Averna M, Calandra S.
Bertolini S, et al.
Atherosclerosis. 2013 Apr;227(2):342-8. doi: 10.1016/j.atherosclerosis.2013.01.007. Epub 2013 Jan 19.
Atherosclerosis. 2013.
PMID: 23375686
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Molecular spectrum of autosomal dominant hypercholesterolemia in France.
Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network; Boileau C, Varret M, Rabès JP.
Marduel M, et al.
Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348.
Hum Mutat. 2010.
PMID: 20809525
Free PMC article.
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Analysis of LDLR variants from homozygous FH patients carrying multiple mutations in the LDLR gene.
Jiang L, Benito-Vicente A, Tang L, Etxebarria A, Cui W, Uribe KB, Pan XD, Ostolaza H, Yang SW, Zhou YJ, Martin C, Wang LY.
Jiang L, et al.
Atherosclerosis. 2017 Aug;263:163-170. doi: 10.1016/j.atherosclerosis.2017.06.014. Epub 2017 Jun 8.
Atherosclerosis. 2017.
PMID: 28645073
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