Prime

Type your tag names separated by a space and hit enter

Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency.

Links

  • Publisher Full Text
  • Authors+Show Affiliations

    ,

    Department of Pediatrics, Hokkaido University Graduate School of Medicine Department of Pediatrics, KKR Sapporo Medical Center, Sapporo, Japan. okura@med.hokudai.ac.jp

    , , , , , ,

    Source

    MeSH

    Child, Preschool
    Codon, Nonsense
    Complement C3
    Exons
    Heterozygote
    Humans
    Male
    Metabolism, Inborn Errors
    Mutation
    RNA Splice Sites
    Sequence Analysis, DNA

    Pub Type(s)

    Case Reports
    Journal Article
    Research Support, Non-U.S. Gov't

    Language

    eng

    PubMed ID

    21501302