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Stephen J. Perkins
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Journal Articles

Autosomal dominant reticuloendothelial iron overload associated with a 3–base pair deletion in the ferroportin 1 gene (SLC11A3)

Clinical Trials & Observations Brief Report
Vinod Devalia, Kymberley Carter, Ann P. Walker, Stephen J. Perkins, Mark Worwood, Alison May, James S. Dooley
Journal: Blood
Blood (2002) 100 (2): 695–697.
https://doi.org/10.1182/blood-2001-11-0132
Published: 2002
Journal Articles

Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15–base pair insertion in the F7 gene

Flora Peyvandi, Josephine A. Carew, David J. Perry, Mathilde Hunault, Uma Khanduri, Stephen J. Perkins, Pier M. Mannucci, Kenneth A. Bauer
Journal: Blood
Blood (2001) 97 (4): 960–965.
https://doi.org/10.1182/blood.V97.4.960
Published: 2001
Journal Articles

Molecular Modeling of Ligand and Mutation Sites of the Type A Domains of Human von Willebrand Factor and Their Relevance to von Willebrand's Disease

P. Vincent Jenkins, K. John Pasi, Stephen J. Perkins
Journal: Blood
Blood (1998) 91 (6): 2032–2044.
https://doi.org/10.1182/blood.V91.6.2032
Published: 1998