Associated Papers
Proteomic Analyses in COVID-19-Associated Secondary Hemophagocytic Lymphohistiocytosis.
Canny SP et al.
Critical Care Explorations, 2025
39888602 (PubMed )
Supplement: cc9-7-e1203-s001.pdf
Identification of biomarkers for COVID-19 associated secondary hemophagocytic lymphohistiocytosis.
Canny SP et al.
Biorxiv : the Preprint Server for Biology, 2024
Enterokinase deficiency with novel TMPRSS15 gene mutation masquerading as acrodermatitis enteropathica.
Chen Y et al.
Pediatric Dermatology, 2023
Workflow for the Implementation of Precision Genomics in Healthcare.
Mehandziska S et al.
Frontiers in Genetics, 2020
32695137 (PubMed )
Supplement: Data_Sheet_2.XLSX › Rare_diseases
Novel Compound Heterozygous TMPRSS15 Gene Variants Cause Enterokinase Deficiency.
Wang L et al.
Frontiers in Genetics, 2020
Comprehensive genomic analyses of a metastatic colon cancer to the lung by whole exome sequencing and gene expression analysis.
Fang LT et al.
International Journal of Oncology, 2014
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.
Holzinger A et al.
American Journal of Human Genetics, 2002
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