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Molecular basis of inherited human antithrombin...
Journal article

Molecular basis of inherited human antithrombin deficiency

Abstract

Figures 1 and 4 summarize the various AT mutations that have been described. The molecular elucidation, over the past decade, of the various AT deficiency types has provided important new insights into functional-structural relationships of AT. This knowledge, together with data provided by monoclonal antibodies and x-ray crystallographic studies of related molecules, has provided important new insights as to how the AT molecule functions in …

Authors

Blajchman M; Austin R; Fernandez-Rachubinski F; Sheffield W

Journal

Blood, Vol. 80, No. 9, pp. 2159–2171

Publisher

American Society of Hematology

Publication Date

November 1, 1992

DOI

10.1182/blood.v80.9.2159.bloodjournal8092159

ISSN

0006-4971