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Updated: Aug 15, 2026

06:33
Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Identification of the novel signal peptide mutation, antithrombin-Siriraj causes type-I antithrombin deficiency in
Yingyong Chinthammitr1, Worrawut Chinchang, Theera Ruchutrakool
1Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands. Y.Y.Chinthammitr@lumc.nl
Thrombosis and Haemostasis
|November 5, 2005
Abstract
No abstract available in PubMed .
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