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Membranoproliferative glomerulonephritis and a rare bleeding disorder: factor X deficiency

✍ Scribed by T. Basturk; E. Ahbap; B. Eroglu Kesim; M. Yılmaz; Y. Koç; T. Sakacı; A. Unsal


Publisher
Springer Netherlands
Year
2010
Tongue
English
Weight
331 KB
Volume
43
Category
Article
ISSN
0301-1623

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## Abstract The combined presence in the homozygous state of more than one recessively transmitted coagulation defect may rarely occur in countries with a high rate of consanguinity. In an Iranian family consisting of two parents (second cousins) and two affected siblings, initial phenotypic analys