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UnknownThe genetic basis of familial hypercholesterolemia: inheritance, linkage, and mutations.
Not available
S-EPMC3681164 | biostudies-literature
UnknownIncreased glycolipid storage produced by the inheritance of a complex intronic haplotype in the α-galactosidase A (GLA) gene.
Not available
S-EPMC4558912 | biostudies-literature
UnknownGenetic Variants of LDLR and PCSK9 Associated with Variations in Response to Antihypercholesterolemic Effects of Armolipid Plus with Berberine.
Not available
S-EPMC4807809 | biostudies-literature
UnknownThe influence of genetic variability and proinflammatory status on the development of bone disease in patients with Gaucher disease.
Not available
S-EPMC4433334 | biostudies-literature
UnknownA genetic variant in the LDLR promoter is responsible for part of the LDL-cholesterol variability in primary hypercholesterolemia.
Not available
S-EPMC4021749 | biostudies-literature
UnknownDiagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease.
Not available
S-EPMC5415726 | biostudies-literature
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