Pathogenic variants of PROC gene caused type II activity deficiency in a Chinese family: A case report

RATIONALE: Hereditary Protein C (PC) deficiency is a rare genetic disorder caused by PROC gene mutation. In this article, we report a case of PC deficiency in a Chinese family due to a novel PROC gene mutation. STUDY SUBJECT: The proband presented with recurrent cerebral infarction over the course o...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Hui, Liu, Hongchao, Liu, Jingyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282035/
https://www.ncbi.nlm.nih.gov/pubmed/33761690
http://dx.doi.org/10.1097/MD.0000000000025160

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282035/
https://www.ncbi.nlm.nih.gov/pubmed/33761690
http://dx.doi.org/10.1097/MD.0000000000025160

Ejemplares similares