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Article

Protein C (PROC) gene mutations in two Indian families with purpura fulminans.

Annals of hematology - 1 Aug 2010

Pai Navin, Shetty Shrimati, Ghosh Kanjaksha

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 20077116
DOI: 10.1007/s00277-009-0893-5

Genes

PROC

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Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Protein C (PROC) gene mutations in two Indian families with purpura fulminans.PMID 20077116Read ↗

A Novel Protein C Mutation Causing Neonatal Purpura Fulminans.Semantic proximity Read ↗

A novel compound heterozygous mutations in protein C gene causing neonatal purpura fulminans.Semantic proximity Read ↗

A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy.Semantic proximity Read ↗

Severe protein C deficiency from compound heterozygous mutations in the PROC gene in two Korean adult patients.Semantic proximity Read ↗

A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period.Semantic proximity Read ↗

Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.Semantic proximity Read ↗

[Analysis of PROC gene variant in a Chinese pedigree affected with hereditary protein C deficiency].Semantic proximity Read ↗

Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.Semantic proximity Read ↗

Mutations in PYCR1 gene in three families with autosomal recessive cutis laxa, type 2.Semantic proximity Read ↗

[Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene].Semantic proximity Read ↗

[Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency].Semantic proximity Read ↗

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

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