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Evaluation of DHPLC in the analysis of hemophilia A

Oldenburg, J, Ivaskevicius, V, Rost, S, Fregin, A, White, K, Holinski-Feder, E, Müller-Reible, C R and Weber, Bernhard H. F. (2001) Evaluation of DHPLC in the analysis of hemophilia A. Journal of Biochemical and Biophysical Methods 47 (1-2), pp. 39-51.

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Abstract

The manifestation of hemophilia A, a common hereditary bleeding disorder in humans, is caused by abnormalities in the factor VIII (FVIII) gene. A wide range of different mutations has been identified and provides the genetic basis for the extensive variability observed in the clinical phenotype. The knowledge of a specific mutation is of great interest as this may facilitate genetic counseling ...

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Item type:Article
Date:2001
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1016/S0165-022X(00)00150-0DOI
Keywords:Hemophilia A; Factor VIII gene; Mutation analysis; DHPLC
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:No
Item ID:35824
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