Analytical Validation of Familial Hypercholesterolemia Biomarkers in Dried Blood Spots

Heterozygous familial hypercholesterolemia (HeFH) is a common, treatable genetic disorder characterized by premature atherosclerosis and cardiovascular disease, yet the majority of affected individuals remain undiagnosed. Newborn screening could play a role in identification of at-risk individuals a...

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Detalles Bibliográficos
Autores principales: Held, Patrice K., Campbell, Kristin, Wiberley-Bradford, Amy E., Lasarev, Michael, Horner, Vanessa, Peterson, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883967/
https://www.ncbi.nlm.nih.gov/pubmed/35225936
http://dx.doi.org/10.3390/ijns8010014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883967/
https://www.ncbi.nlm.nih.gov/pubmed/35225936
http://dx.doi.org/10.3390/ijns8010014

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