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A small deletion in SERPINC1 causes type I antithrombin deficiency by promoting endoplasmic reticulum stress
Antithrombin (AT) deficiency is an autosomal dominant disorder, and identification of mutation AT variants would improve our understanding of the anticoagulant function of this serine protease inhibitor (SERPIN) and the molecular pathways underlying this disorder. In the present study, we performed...
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| Publicado no: | Oncotarget |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Impact Journals LLC
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5363556/ https://ncbi.nlm.nih.gov/pubmed/27708219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.12349 |
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