Antithrombin III alger: A new case of Arg 47 ← cys mutation
Author:
Publisher
Wiley
Subject
Hematology
Reference7 articles.
1. Antithrombin III Alger: A New Homozygous AT III Variant
2. Antithrombin III Toyama: replacement of arginine-47 by cysteine in hereditary abnormal antithrombin III that lacks heparin-binding ability.
3. Antithrombin III Tours gene: Identification of a point mutation leading to an arginine—cysteine replacement in a silent deficiency
4. Antithrombin III Basel. Identification of a Pro-Leu substitution in a hereditary abnormal antithrombin with impaired heparin cofactor activity.
5. The heparin-binding site of antithrombin III. Identification of a critical tryptophan in the amino acid sequence.
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