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1 Matching Annotations
  1. Oct 2026
  2. www.sciencedirect.com www.sciencedirect.com
    Molecular study of VWF gene from Mexican Mestizo patients with von Willebrand disease, and the finding of three new mutations
    1
    1. ClingenBaseline 25 Oct 2026
      in Baseline Annotations
      The S1285F mutation alters the folding of A1 loop and avoids the exposure of the VWF protein to platelets. This substitution was detected in a 2M patient and her mother.
      CA114164 inferred_gene_hgnc:12726 inferred_gene_source:CAID ClinGen VWF
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    Tags

    • inferred_gene_source:CAID
    • inferred_gene_hgnc:12726
    • CA114164
    • ClinGen VWF

    Annotators

    • ClingenBaseline

    URL

    sciencedirect.com/science/article/pii/S1079979607001234
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