A de novo mutation in exon 28 of the von Willebrand factor gene in a patient with type IIA von Willebrand's disease coincides with an Mbol polymorphism in the von Willebrand factor pseudogene

Journal Article A de novo mutation in exon 28 of the von Willebrand factor gene in a patient with type IIA von Willebrand's disease coincides with an Mbol polymorphism in the von Willebrand factor pseudogene Get access Margarita Pérez-Casal, Margarita Pérez-Casal * Section of Molecular Genetics, Department of Medicine and Pharmacology, Royal Hallamshire HospitalGlossop Road, Sheffield S10 2JF, UK *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Martina Daly, Martina Daly Section of Molecular Genetics, Department of Medicine and Pharmacology, Royal Hallamshire HospitalGlossop Road, Sheffield S10 2JF, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar an Peake an Peake Section of Molecular Genetics, Department of Medicine and Pharmacology, Royal Hallamshire HospitalGlossop Road, Sheffield S10 2JF, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 2, Issue 12, December 1993, Pages 2159–2161, https://doi.org/10.1093/hmg/2.12.2159 Published: 01 December 1993 Article history Received: 16 August 1993 Revision received: 20 September 1993 Accepted: 20 September 1993 Published: 01 December 1993