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Thromb Haemost 1998; 79(06): 1215-1216
DOI: 10.1055/s-0037-1615044
DOI: 10.1055/s-0037-1615044
Letters to the Editor
Protein C Gene Polymorphism and Hypertensive Cerebrovascular Disease in Japanese
Further Information
Publication History
Received
15 January 1998
Accepted
13 February 1998
Publication Date:
07 December 2017 (online)
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References
- 1 Spek CA, Koster T, Rosendaal FR, Bertina RM, Reitsma PH. Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk.. Arterioscler Thromb Vasc Biol 1995; 15: 214-8.
- 2 Kario K, Matsuo T, Kobayashi H, Asada R, Matsuo M. “Silent” cerebral infarction is associated with hypercoagulability, endothelial cell damage, and high Lp(a) levels in elderly Japanese.. Arterioscler Thromb Vasc Biol 1996; 16: 734-41.
- 3 Kario K, Kanai N, Saito K, Nago N, Matsuo T, Shimada K. Ischemic stroke and the gene for angiotensin-converting enzyme in Japanese hypertensives.. Circulation 1996; 93: 1630-3.
- 4 Shiga N, Takeshima Y, Sakamoto H, Inoue K, Yokota Y, Yokoyama M, Matsuo M. Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.. J Clin Invest 1998; 100: 2204-10.
- 5 Fujimura H, Kambayashi J, Monden M, Kato H, Miyata T. Coagulation factor V Leiden mutation may have a racial background.. Thromb Haemost 1995; 74: 1381-2.