DOI: 10.1055/s-00000077

Seminars in Thrombosis and Hemostasis

References

Lombardi AM, Bortoletto E, Scarparo P, Scapin M, Santarossa L, Girolami A.
Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.

Blood Coagul Fibrinolysis 2008;
19 (07) 639-643

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