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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Detalles Bibliográficos
Autores principales: Su, Jingjing, Shu, Liang, Zhang, Zhou, Cai, Lei, Zhang, Xin, Zhai, Yu, Liu, Jianren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363556/
https://www.ncbi.nlm.nih.gov/pubmed/27708219
http://dx.doi.org/10.18632/oncotarget.12349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363556/
https://www.ncbi.nlm.nih.gov/pubmed/27708219
http://dx.doi.org/10.18632/oncotarget.12349

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