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Small insertion (c.869insC) within F13A gene is dominant in Tunisian patients with inherited FXIII deficiency due to ancient founder effect

✍ Scribed by H. EL MAHMOUDI; M. B. AMOR; E. GOUIDER; R. HORCHANI; R. HAFSIA; K. FADHLAOUI; B. MEDDEB; A. HAFSIA; A. B. AMMAR EL GAAIED


Book ID
108775296
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
94 KB
Volume
15
Category
Article
ISSN
1351-8216

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