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Genotype and Laboratory and Clinical Phenotypes of Protein S Deficiency
Duebgen, Sebastian, Kauke, Teresa, Marschall, Christoph, Giebl, Andreas, Lison, Susanne, Hart, Christina, Dick, Andrea and Spannagl, Michael (2012) Genotype and Laboratory and Clinical Phenotypes of Protein S Deficiency. American Journal of Clinical Pathology 137 (2), pp. 178-184.Date of publication of this fulltext: 19 Dec 2024 09:43
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| Item type | Article | ||||
| Journal or Publication Title | American Journal of Clinical Pathology | ||||
| Publisher: | AMER SOC CLINICAL PATHOLOGY | ||||
|---|---|---|---|---|---|
| Place of Publication: | CHICAGO | ||||
| Volume: | 137 | ||||
| Number of Issue or Book Chapter: | 2 | ||||
| Page Range: | pp. 178-184 | ||||
| Date | 2012 | ||||
| Institutions | Medicine > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie) | ||||
| Identification Number |
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| Keywords | PATENT FORAMEN OVALE; YOUNG STROKE PATIENTS; POINT MUTATIONS; MOLECULAR-BASIS; FREQUENT MUTATION; PROS1 GENE; FACTOR-V; FAMILIES; IDENTIFICATION; THROMBOPHILIA; Protein S deficiency; PROS1; Genotype; Phenotype; Laboratory assessment | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 64105 |
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