Rare and common variants of APOB and PCSK9 in Korean patients with extremely low low-density lipoprotein-cholesterol levels

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Rare and common variants of APOB and PCSK9 in Korean patients with extremely low low-density lipoprotein-cholesterol levels

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Rare and common variants of AP ...... lipoprotein-cholesterol levels

@en

Rare and common variants of AP ...... lipoprotein-cholesterol levels

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Item

label

Rare and common variants of AP ...... lipoprotein-cholesterol levels

@en

Rare and common variants of AP ...... lipoprotein-cholesterol levels

@nl

prefLabel

Rare and common variants of AP ...... lipoprotein-cholesterol levels

@en

Rare and common variants of AP ...... lipoprotein-cholesterol levels

@nl

P1476

Rare and common variants of AP ...... lipoprotein-cholesterol levels

@en

P2093

Chan Joo Lee

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Ji Hyun Lee

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Yunbeom Lee

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P2860

Molecular diagnosis of hypobetalipoproteinemia: an ENID review

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

A common PCSK9 haplotype, encompassing the E670G coding single nucleotide polymorphism, is a novel genetic marker for plasma low-density lipoprotein cholesterol levels and severity of coronary atherosclerosis.

A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

Update on the molecular biology of dyslipidemias.

High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descent.

Hypobetalipoproteinemia and abetalipoproteinemia.

Monogenic hypocholesterolaemic lipid disorders and apolipoprotein B metabolism.

Differential effects of PCSK9 loss of function variants on serum lipid and PCSK9 levels in Caucasian and African Canadian populations.

Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease.

P304

e0186446

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scholarly article

P356

10.1371/JOURNAL.PONE.0186446

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P407

English

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P478

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P577

2017-10-16T00:00:00Z

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P698

29036232

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P932

5643101

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