𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular basis for factor H and FHL-1 deficiency in an Italian family

✍ Scribed by P. Sánchez-Corral; D. Bellavia; L. Amico; M. Brai; S. Rodríguez de Córdoba


Book ID
105948825
Publisher
Springer-Verlag
Year
2000
Tongue
English
Weight
109 KB
Volume
51
Category
Article
ISSN
0093-7711

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Homozygous hereditary C1q deficiency and
✍ Jason H. Slingsby; Peter Norsworthy; Glen Pearce; Akshay K. Vaishnaw; Helen Issl 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 739 KB

Objective. To describe a new kindred with Clq deficiency and to identify the molecular lesions responsible for complete functional Clq deficiency in this and 2 other previously described kindreds. Methods. The A-, B-, and C-chain genes of Clq were amplified by polymerase chain reaction, cloned, and

Molecular basis of inherited antithrombi
✍ Dezsö David; Sofia Ribeiro; Lénia Ferrão; Teresa Gago; Francisco Crespo 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 309 KB 👁 1 views

## Abstract Antithrombin (AT), the most important coagulation serine proteases inhibitor, plays an important role in maintaining the hemostatic balance. Inherited AT deficiency, mainly characterized by predisposition to recurrent venous thromboembolism, is transmitted in an autosomal dominant manne