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Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.

Annals of hematology - 1 Feb 2024

Xu Fei, Zhang Ke, Xu Qiyu, Ye Longying, Zeng Manlin, Jin Yanhui, Wang Mingshan, Yang Lihong

Abstract excerpt

Currently, limited information is available in the literature regarding the relationships between PROC mutations and clinical features in Chinese individuals. We aimed to characterize severe congenital Protein C deficiency in 22 unrelated Chinese families in a tertiary hospital by analyzing its clinical manifestation, associated risk factors, and gene mutations. We measured protein C activity and antigen levels...

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PMID: 37950050
DOI: 10.1007/s00277-023-05487-w

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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