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Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis

✍ Scribed by Lena Tjeldhorn; Per Morten Sandset; Kaia Haugbro; Grethe Skretting

Book ID: 116914145
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 206 KB
Volume: 125
Category: Article
ISSN: 0049-3848
DOI: 10.1016/j.thromres.2009.05.013

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