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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Last data update: Apr 19, 2024
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Abnormalities and LDLR[original query]
Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients.
Human genetics 2003 Dec 114 (1): 87-98.
McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J,
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Increased intestinal cholesterol absorption in autosomal dominant hypercholesterolemia and no mutations in the low-density lipoprotein receptor or apolipoprotein B genes.
The Journal of clinical endocrinology and metabolism 2007 Sep 92 (9): 3667-73.
García-Otín A L, Cofán M, Junyent M, Recalde D, Cenarro A, Pocoví M, Ros E, Civeira
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Detection of mutations and large rearrangements of the low-density lipoprotein receptor gene in Taiwanese patients with familial hypercholesterolemia.
The American journal of cardiology 2010 Jun 105 (12): 1752-8.
Chiou Kuan-Rau, Charng Min-
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Clinical and serum lipid profiles and LDLR genetic analysis of xanthelasma palpebrarum with nonfamilial hypercholesterolemia.
Journal of cosmetic dermatology 2020 3 19 (11): 3096-3099.
Zhimin Wang, Hui Wang, Fengtao Ji, Wenjuan Sun, Yongrong
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Differential distribution of gene polymorphisms associated with hypercholesterolemia, hypertriglyceridemia, and hypoalphalipoproteinemia among Native American and Mestizo Mexicans.
World journal of hepatology 2022 9 14 (7): 1408-1420.
Torres-Valadez Rafael, Roman Sonia, Ojeda-Granados Claudia, Gonzalez-Aldaco Karina, Panduro Artu
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 16, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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