𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular basis of factor X deficiency cases from India

✍ Scribed by L. MOTA; S. SHETTY; S. IDICULA-THOMAS; K. GHOSH


Book ID
108775447
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
243 KB
Volume
16
Category
Article
ISSN
1351-8216

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Molecular genetic analysis of factor X d
✍ Kerstin Wieland; David S. Millar; Catherine B. Grundy; Reuben S. Mibashan; Vijay πŸ“‚ Article πŸ“… 1991 πŸ› Springer 🌐 English βš– 882 KB

A case of homozygous factor X deficiency arising from the inheritance of two non-identical gene deletions from heterozygous parents is described. One, a partial gene deletion, was localized to exons VII and VIII by a combination of Southern blotting and polymerase chain reaction (PCR) amplification