A carregar...
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...
Na minha lista:
| Publicado no: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7685646/ https://ncbi.nlm.nih.gov/pubmed/33228548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01176-x |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|