Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a)
- DOI
- 10.1016/s0049-3848(01)00406-6
- Published
- 2002-01
- Container
- Thrombosis Research
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/s0049-3848-01-00406-6,
title = {Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a)},
author = {Andrea Kosch and Ralf Junker and Cornelia Wermes and Ulrike Nowak-Göttl},
year = {2002},
journal = {Thrombosis Research},
doi = {10.1016/s0049-3848(01)00406-6},
url = {https://doi.org/10.1016/s0049-3848(01)00406-6}
}RIS
TY - JOUR TI - Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a) AU - Andrea Kosch AU - Ralf Junker AU - Cornelia Wermes AU - Ulrike Nowak-Göttl PY - 2002 JO - Thrombosis Research DO - 10.1016/s0049-3848(01)00406-6 UR - https://doi.org/10.1016/s0049-3848(01)00406-6 ER -
APA
Kosch, A., Junker, R., Wermes, C., & Nowak-Göttl, U. (2002). Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a). Thrombosis Research. https://doi.org/10.1016/s0049-3848(01)00406-6
Source records
- crossref · retrieved 2026-09-27T05:04:08.037Z