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Thromb Haemost 2006; 95(05): 893-895
DOI: 10.1160/TH06-01-0051
DOI: 10.1160/TH06-01-0051
Case Report
Combined factor V – factor VIII deficiency (F5F8D): Compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient
Authors
Financial support: This study was supported by the Swiss National Science Foundation (SNF). MNA is the recipient of an SNF Professorship (# 631–66023).
Further Information
Publication History
Received
25 January 2006
Accepted after resubmission
16 March 2006
Publication Date:
01 December 2017 (online)
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References
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