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Year | Number of Results |
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1992 | 2 |
1993 | 1 |
2024 | 0 |
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Screening for the apolipoprotein B-100 arginine3500-->glutamine mutation in patients with type III hyperlipoproteinemia.
Clin Genet. 1992 Dec;42(6):302-5. doi: 10.1111/j.1399-0004.1992.tb03260.x.
Clin Genet. 1992.
PMID: 1493642
Familial defective apolipoprotein B-100: mild hypercholesterolaemia without atherosclerosis in a homozygous patient.
März W, Ruzicka C, Pohl T, Usadel KH, Gross W.
März W, et al.
Lancet. 1992 Nov 28;340(8831):1362. doi: 10.1016/0140-6736(92)92554-s.
Lancet. 1992.
PMID: 1360085
No abstract available.
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Accumulation of "small dense" low density lipoproteins (LDL) in a homozygous patients with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor.
März W, Baumstark MW, Scharnagl H, Ruzicka V, Buxbaum S, Herwig J, Pohl T, Russ A, Schaaf L, Berg A, et al.
März W, et al.
J Clin Invest. 1993 Dec;92(6):2922-33. doi: 10.1172/JCI116915.
J Clin Invest. 1993.
PMID: 8254047
Free PMC article.
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