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British Journal of Haematology|January 26, 2005
Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletionJeff Hewitt, Jennifer N M Ballard, Tanya N Nelson, et al.Proceedings of the National Academy of Sciences of the United States of America|October 23, 2002
Permanent and panerythroid correction of murine beta thalassemia by multiple lentiviral integration in hematopoietic stem cellsSuzan Imren, Emmanuel Payen, Karen A Westerman, et al.Brain : a Journal of Neurology|September 2, 2008
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international seriesT E F Webb, M Poulter, J Beck, et al.ACS Infectious Diseases|November 22, 2022
Synthesis, Antibacterial Activity, and Nephrotoxicity of Polymyxin B Analogues Modified at Leu-7, d-Phe-6, and the N-Terminus Enabled by S-LipidationPaul W R Harris, Andrew Siow, Sung-Hyun Yang, et al.Pageof 21