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Dominant type 1 vonWillebrand's disease as a result of a deletion of a single codon in exon 28 of the VWF gene [Abstract]

Jenkins, P. V., Ononye, C., Collins, Peter William ORCID: https://orcid.org/0000-0002-6410-1324 and Pasi, K. J. 1996. Dominant type 1 vonWillebrand's disease as a result of a deletion of a single codon in exon 28 of the VWF gene [Abstract]. British Journal of Haematology 93 (S2) , 1176.

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Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Systems Immunity Research Institute (SIURI)
Subjects: Q Science > QH Natural history > QH426 Genetics
R Medicine > R Medicine (General)
Publisher: Wiley-Blackwell
ISSN: 0007-1048
Related URLs:
Last Modified: 27 Oct 2022 10:27
URI: https://orca.cardiff.ac.uk/id/eprint/70395

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