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An analysis of 8 cases of factor X deficiency

โœ Scribed by Nilam M. Shah; Ashwin P. Patel


Book ID
107645289
Publisher
Springer-Verlag
Year
2008
Tongue
English
Weight
53 KB
Volume
24
Category
Article
ISSN
0971-4502

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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