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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
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Genetic Screening of LCA in Belgium: Predominance of CEP290 and Identification of Potential Modifier Alleles in AHI1 of CEP290-Related Phenotypes
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Genetically Confirmed Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome