Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study-Reference-Cited by-同舟云学术

Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study

Author:

Kumar Riten¹,Chan Anthony K. C.²,Dawson Jennifer E.³⁴,Forman-Kay Julie D.³⁴,Kahr Walter H. A.⁴⁵⁶,Williams Suzan⁶

Affiliation:

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

2. Department of Paediatrics; Division of Haematology/Oncology; McMaster Children's Hospital; McMaster University; Toronto ON USA

3. Program in Molecular Structure and Function; Research Institute; The Hospital for Sick Children; Toronto ON USA

4. Department of Biochemistry; University of Toronto; Toronto ON USA

5. Program in Cell Biology; Research Institute; The Hospital for Sick Children; Toronto ON USA

6. Department of Paediatrics; Division of Haematology, Oncology; The Hospital for Sick Children; University of Toronto; Toronto ON USA

Publisher

Wiley

Subject

Hematology

Link

Reference45 articles.

1. Inherited antithrombin III deficiency and cerebral thrombosis in a child;Ambruso;Pediatrics,1980

4. Electrostatics of nanosystems: application to microtubules and the ribosome;Baker;Proceedings of the National Academy of Sciences of the United States of America,2001

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