Molecular structural analysis of a novel and de-novo mutation in theSERPINC1gene associated with type 1 antithrombin deficiency-Reference-Cited by-同舟云学术

Molecular structural analysis of a novel and de-novo mutation in theSERPINC1gene associated with type 1 antithrombin deficiency

Author:

Wang Tzu-Fei¹,Dawson Jennifer E.²³,Forman-Kay Julie. D.²³,Kahr Walter H. A.³⁴⁵,Williams Suzan⁵,Chan Anthony K.⁶,Kumar Riten⁷

Affiliation:

1. Department of Internal Medicine; Division of Hematology; The Ohio State University; Columbus OH USA

2. Program in Molecular Structure and Function, Research Institute; The Hospital for Sick Children; Toronto ON Canada

3. Department of Biochemistry; University of Toronto; ON Canada

4. Program in Cell Biology, Research Institute; The Hospital for Sick Children; Toronto ON Canada

5. Department of Paediatrics; Division of Haematology/Oncology; The Hospital for Sick Children; University of Toronto; Toronto ON Canada

6. Department of Paediatrics; Division of Haematology/Oncology; McMaster Children's Hospital; McMaster University; Hamilton ON Canada

7. Department of Pediatrics; Division of Hematology/Oncology; Nationwide Children's Hospital; The Ohio State University; Columbus OH USA

Publisher

Wiley

Subject

Hematology

Link

Reference8 articles.

5. Molecular basis of antithrombin deficiency;Luxembourg;Thrombosis and Haemostasis,2011

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