ArticleInternational journal of molecular sciences2025
Clinical and Genetic Heterogeneity of Factor XI Deficiency: Insights from a Southern Italian Cohort.
Rosa Santacroce, Giovanna D'Andrea, Giovanni Luca Tiscia, Giuseppe Lassandro, Maria d'Apolito, Doris Barcellona, Patrizia De Bonis, Francesco Marongiu, Paola Giordano, Elvira Grandone and 1 more
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In one paragraphArticle in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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What it found
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2 · The registryThe trial behind it
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3 · Its place in the literatureWho cites it
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4 · The recordCorrections and comments
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5 · Who and what moneyAuthors and funding
11 authors.
Rosa SantacroceMedical Genetics, Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Giovanna D'AndreaMedical Genetics, Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Giovanni Luca TisciaThrombosis and Haemostasis Unit, Fondazione IRCCS "Casa Sollievo della Sofferenza", Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0001-5896-2024 Giuseppe LassandroDepartment of Biomedical Sciences and Human Oncology, Pediatric Section, University of Bari "A. Moro", 70126 Bari, Italy.
Maria d'ApolitoMedical Genetics, Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.ORCID 0000-0001-9170-4668 Doris BarcellonaDepartment of Medical Science and Public Health, University of Cagliari, 09124 Cagliari, Italy.ORCID 0000-0002-0823-3357 Patrizia De BonisThrombosis and Haemostasis Unit, Fondazione IRCCS "Casa Sollievo della Sofferenza", Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.
Francesco MarongiuDepartment of Medical Science and Public Health, University of Cagliari, 09124 Cagliari, Italy.
Paola GiordanoDepartment of Biomedical Sciences and Human Oncology, Pediatric Section, University of Bari "A. Moro", 70126 Bari, Italy.
Elvira GrandoneThrombosis and Haemostasis Unit, Fondazione IRCCS "Casa Sollievo della Sofferenza", Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-8980-9783 Maurizio MargaglioneMedical Genetics, Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.ORCID 0000-0001-5627-9221 Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
Factor XI (FXI) deficiency, or hemophilia C, is a rare bleeding disorder resulting from reduced levels or dysfunctional FXI protein due to mutations in the
Indexed as
Factor XIFactor XI DeficiencyGenetic HeterogeneityAdolescentAdultAgedChildChild, PreschoolCohort StudiesFemaleGenetic Association StudiesGenotypeHumansItalyMaleMiddle AgedFactor XIbleedingFXI deficiencygene variantlevelsphenotype
Identifiers
PMID41009375
PMCPMC12469505
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