(Q34679770)

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Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

0 references

1 reference

based on heuristic

inferred from title

John J. P. Kastelein

7

object named as

J J P Kastelein

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

author name string

D M Kusters

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

R Huijgen

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

J C Defesche

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

M N Vissers

4

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

I Kindt

5

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

B A Hutten

6

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

publication date

27 January 2011

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Netherlands Heart Journal

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

19

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Europe PubMed Central

PubMed publication ID

3 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

175-182

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Two years after molecular diagnosis of familial hypercholesterolemia: majority on cholesterol-lowering treatment but a minority reaches treatment goal

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Familial hypercholesterolemia: current treatment and advances in management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Origin and migration of an Afrikaner founder mutation FHAfrikaner-2 (V408M) causing familial hypercholesterolemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Estimation of the prevalence of familial hypercholesterolaemia in a rural Afrikaner community by direct screening for three Afrikaner founder low density lipoprotein receptor gene mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Evaluation of the Cholestech L.D.X. desktop analyser for cholesterol, HDL-cholesterol, and triacylglycerols in heparinized venous blood.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058324

7 July 2018

Update and analysis of the University College London low density lipoprotein receptor familial hypercholesterolemia database

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0076-6

21 January 2018

Functionality of sequence variants in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in individuals with inherited hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0076-6

21 January 2018

Low-density lipoprotein receptor gene mutations and cardiovascular risk in a large genetic cascade screening population

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0076-6

21 January 2018

Update of the molecular basis of familial hypercholesterolemia in The Netherlands

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0076-6

21 January 2018

South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0076-6

21 January 2018

Impact of low-density lipoprotein receptor mutational class on carotid atherosclerosis in patients with familial hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0076-6

21 January 2018

The molecular basis of familial hypercholesterolemia in The Netherlands

1 reference

https://pubmed.ncbi.nlm.nih.gov/21475731

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low-density lipoprotein receptor gene mutations in a Southeast Asian population with familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21475731

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the age of the ancestral arginine3500-->glutamine mutation in human apoB-100

1 reference

https://pubmed.ncbi.nlm.nih.gov/21475731

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis of familial hypercholesterolemia: spectrum and regional difference of LDL receptor gene mutations in Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21475731

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Higher prevalence of familial hypercholesterolemia than expected in adult patients of four family practices in Netherlands]

1 reference

https://pubmed.ncbi.nlm.nih.gov/21475731

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years]

1 reference

https://pubmed.ncbi.nlm.nih.gov/21475731

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12471-011-0076-6

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Dimensions Publication ID

0 references

release_akjrkfbqy5d73gqie6dcnfmhgy

1 reference

https://api.fatcat.wiki/v0/release/akjrkfbqy5d73gqie6dcnfmhgy

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

ResearchGate publication ID

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