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4. Spectrum of mutations in homozygous familial hypercholesterolemia in India, with four novel mutations. Setia N, Saxena R, Arora A, Verma IC. Atherosclerosis; 2016 Dec; 255():31-36. PubMed ID: 27816806 [Abstract] [Full Text] [Related]
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11. Health related quality of life in individuals at high risk for familial hypercholesterolemia undergoing genetic cascade screening in Brazil. Souto AC, Miname MH, Fukushima J, Jannes CE, Krieger JE, Hagger M, Pereira AC, Santos RD. Atherosclerosis; 2018 Oct 12; 277():464-469. PubMed ID: 30270086 [Abstract] [Full Text] [Related]
12. Independent Severe Cases of Heterozygous Familial Hypercholesterolemia Caused by the W483X and Novel W483G Mutations in the Low-Density Lipoprotein Receptor Gene That Were Clinically Diagnosed as Homozygous Cases. Cheng S, Wu Y, Wen W, An M, Gao Y, Wang L, Han X, Shang H. Genet Test Mol Biomarkers; 2019 Jun 12; 23(6):401-408. PubMed ID: 31161821 [Abstract] [Full Text] [Related]
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20. Cascade screening for familial hypercholesterolemia: Practical consequences. Louter L, Defesche J, Roeters van Lennep J. Atheroscler Suppl; 2017 Nov 24; 30():77-85. PubMed ID: 29096865 [Abstract] [Full Text] [Related] Page: [Next] [New Search]