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Article

Paediatric presentation and outcome of congenital protein C deficiency in Japan.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 May 2013

Ohga S, Kang D, Kinjo T, Ochiai M, Doi T, Ishimura M, Kayamori Y, Urata M, Yamamoto J, Suenobu S-I, Kanegane H, Ikenoue T, Shirahata A, Hara T

Abstract excerpt

Severe heritable protein C (PC) deficiency is quite rare, although heterozygous PROC mutation is the second leading cause of genetic predisposition to thrombosis in Japanese adults. The aim of the study was to search the optimal management, the paediatric onset and outcomes of PC deficiency were...

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Identifiers

PMID: 23379934
DOI: 10.1111/hae.12097

Genes

PROC

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23379934-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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