Coagulation Factor IX Propeptide Mutations Causing Coumarin Hypersensitivity: Identification of Female Alanine-10 Valine Heterozygotes
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| Veröffentlicht in: | Thrombosis and haemostasis 2001-03, Vol.85 (3), p.567-568 |
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| container_end_page | 568 |
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| container_issue | 3 |
| container_start_page | 567 |
| container_title | Thrombosis and haemostasis |
| container_volume | 85 |
| creator | BESTMANN, Lukas ZÜGER, Max OLDENBURG, Johannes BÜHLER, Damian MALY, Friedrich E |
| description | |
| doi_str_mv | 10.1055/s-0037-1615629 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0340-6245 |
| ispartof | Thrombosis and haemostasis, 2001-03, Vol.85 (3), p.567-568 |
| issn | 0340-6245 2567-689X |
| language | eng |
| recordid | cdi_crossref_primary_10_1055_s_0037_1615629 |
| source | MEDLINE; Thieme Connect Journals |
| subjects | Biological and medical sciences Coumarins - administration & dosage Coumarins - adverse effects Drug Hypersensitivity - etiology Drug toxicity and drugs side effects treatment Factor IX - genetics Family Health Female Founder Effect Hemorrhage - chemically induced Hemorrhage - genetics Heterozygote Humans Letters to the Editor Male Medical sciences Pharmacology. Drug treatments Point Mutation Toxicity: blood |
| title | Coagulation Factor IX Propeptide Mutations Causing Coumarin Hypersensitivity: Identification of Female Alanine-10 Valine Heterozygotes |
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