Molecular pathogenesis of plasminogen Hakodate: the second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis.
Saved in:
| Title: | Molecular pathogenesis of plasminogen Hakodate: the second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis. |
|---|---|
| Authors: | Osaki T; Department of Molecular Patho-Biochemistry and Patho-Biology, Yamagata University School of Medicine, Iida-Nishi 2-2-2, Yamagata, 990-9585, Japan., Souri M; Department of Molecular Patho-Biochemistry and Patho-Biology, Yamagata University School of Medicine, Iida-Nishi 2-2-2, Yamagata, 990-9585, Japan., Song YS; Department of Ophthalmology, Goryokaku Hospital, Hakodate, Japan., Izumi N; Department of Ophthalmology, Goryokaku Hospital, Hakodate, Japan., Law R; Department of Biochemistry and Molecular Biology, Monash University, Clayton, Melbourne, VIC, 3800, Australia., Ichinose A; Department of Molecular Patho-Biochemistry and Patho-Biology, Yamagata University School of Medicine, Iida-Nishi 2-2-2, Yamagata, 990-9585, Japan. aichinos@med.id.yamagata-u.ac.jp. |
| Source: | Journal of thrombosis and thrombolysis [J Thromb Thrombolysis] 2016 Aug; Vol. 42 (2), pp. 218-24. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Kluwer Academic Publishers Country of Publication: Netherlands NLM ID: 9502018 Publication Model: Print Cited Medium: Internet ISSN: 1573-742X (Electronic) Linking ISSN: 09295305 NLM ISO Abbreviation: J Thromb Thrombolysis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
