Widening the spectrum of genetic testing in familial hypercholesterolaemia: Will it translate into better patient and population outcomes?-Reference-Cited by-同舟云学术

Widening the spectrum of genetic testing in familial hypercholesterolaemia: Will it translate into better patient and population outcomes?

Published:2019-12-27 Issue:4 Volume:97 Page:543-555
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Page Michael M.¹²^ORCID,Bell Damon A.¹³⁴⁵,Watts Gerald F.¹⁴

Affiliation:

1. School of Medicine, Faculty of Medicine and Health SciencesThe University of Western Australia Perth Australia

2. Department of Clinical BiochemistryWestern Diagnostic Pathology Perth Australia

3. Department of Clinical BiochemistryPathWest Fiona Stanley Hospital and Royal Perth Hospital Perth Australia

4. Lipid Disorders Clinic, Department of CardiologyRoyal Perth Hospital Perth Australia

5. Department of Clinical BiochemistryClinipath Pathology Perth Australia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13685

Reference99 articles.

1. Centers for Disease Control and Prevention. Tier 1 genomic applications and their importance to public health.2014;https://www.cdc.gov/genomics/implementation/toolkit/tier1.htm. Accessed 24 September 2019.

2. The complex molecular genetics of familial hypercholesterolaemia

3. Familial hypercholesterolemia in South African Afrikaners

4. The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum ofLDLRmutations and role ofPCSK9as a modifier gene

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

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