For clinicians, geneticists, and scientists who encounter and study the mutations which give rise to disorders of blood coagulation, this monograph brings together all the relevant information which can be used in identifying genetic defects of the coagulation mechanism, as a guide to locating within the hemostatic system the likely effect of any mutation. Alternatively, starting from a case of functional deficiency of any coagulation protein, it directs the researcher along the most likely path to elucidating the underlying genetic defect. Annotation copyright Book News, Inc. Portland, Or.
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