2019
DOI: 10.1097/md.0000000000014247
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Screening of common genetic variants in the APOB gene related to familial hypercholesterolemia in a Saudi population

Abstract: Familial hypercholesterolemia (FH) is a monogenic dominant inherited disorder of lipid metabolism characterized by elevated low-density lipoprotein levels, and is mainly attributable to mutations in low-density lipoprotein receptor (LDLR), apolipoprotein B (APOB), and proportein convertase subtilisin/kexin type 9 (PCSK9) genes. Next-generation and exome sequencing studies have primarily involved genome-wide association analyses, and meta-analyses and next-generation studies examined a few single-nucleotide pol… Show more

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Cited by 6 publications
(1 citation statement)
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“…Apolipoprotein B (APOB) has long been of interest due to its close association with cardiovascular diseases. [12][13][14] However, recent studies have suggested that APOB also plays an important role in the occurrence and progression of various tumors, including hepatocellular carcinoma, 15 kidney renal clear cell carcinoma, 16 nonesophageal squamous cell carcinoma, 17 and breast cancer. 18 However, no study has specifically investigated the prognostic role of APOB in patients with glioma.…”
Section: Introductionmentioning
confidence: 99%
“…Apolipoprotein B (APOB) has long been of interest due to its close association with cardiovascular diseases. [12][13][14] However, recent studies have suggested that APOB also plays an important role in the occurrence and progression of various tumors, including hepatocellular carcinoma, 15 kidney renal clear cell carcinoma, 16 nonesophageal squamous cell carcinoma, 17 and breast cancer. 18 However, no study has specifically investigated the prognostic role of APOB in patients with glioma.…”
Section: Introductionmentioning
confidence: 99%