Mice lacking global Stap1 expression do not manifest hypercholesterolemia

BACKGROUND: Autosomal dominant familial hypercholesterolemia (ADH; MIM#143890) is one of the most common monogenic disorders characterized by elevated circulatory LDL cholesterol. Initial studies in humans with ADH identified a potential relationship with variants of the gene encoding signal transdu...

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Detalles Bibliográficos
Autores principales: Kanuri, Babunageswararao, Fong, Vincent, Haller, April, Hui, David Y., Patel, Shailendra B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685646/
https://www.ncbi.nlm.nih.gov/pubmed/33228548
http://dx.doi.org/10.1186/s12881-020-01176-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685646/
https://www.ncbi.nlm.nih.gov/pubmed/33228548
http://dx.doi.org/10.1186/s12881-020-01176-x

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