Heckathorn disease revisited-Reference-Cited by-同舟云学术

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Heckathorn disease revisited

Published:2014-02-27 Issue:9 Volume:123 Page:1429-1431
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Nand Sucha¹,Barton Kevin¹,Schultz Richard²,Klein Mary³,Kini Ameet⁴

Affiliation:

1. Department of Medicine, Loyola University Medical Center, Maywood, IL

2. Department of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL

3. Porter Hematology Oncology, Valparaiso, IN

4. Department of Pathology, Loyola University Medical Center, Maywood, IL

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/123/9/1429/1378955/1429.pdf

Reference9 articles.

1. Heckathorn’s disease: variable functional dificiency of antihemophilic factor (factor VIII).;Ratnoff;Blood,1975

2. The tertiary structure and domain organization of coagulation factor VIII.;Shen;Blood,2008

3. The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.;Payne;Hum Mutat,2013

4. Molecular genetic testing of hemophilia A.;Goodeve;Semin Thromb Hemost,2008

5. Mild hemophilia A caused by increased rate of factor VIII A2 subunit dissociation: evidence for nonproteolytic inactivation of factor VIIIa in vivo.;Pipe;Blood,1999

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