Associated Papers
Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review.
Zhang Z et al.
Medicine, 2022
Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
Barg AA et al.
Acta Haematologica, 2021
ATP1A3 mosaicism in families with alternating hemiplegia of childhood.
Yang X et al.
Clinical Genetics, 2019
30891744 (PubMed )
Supplement: CGE-96-43-s001.docx
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