The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease (Q24540182)

From Wikidata
Jump to navigation Jump to search
scientific article
edit
Language Label Description Also known as
English
The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease
scientific article

    Statements

    The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease (English)
    0 references
    A Maugeri
    0 references
    M A van Driel
    0 references
    D J van de Pol
    0 references
    B J Klevering
    0 references
    F J van Haren
    0 references
    N Tijmes
    0 references
    A A Bergen
    0 references
    K Rohrschneider
    0 references
    A Blankenagel
    0 references
    A J Pinckers
    0 references
    N Dahl
    0 references
    H G Brunner
    0 references
    A F Deutman
    0 references
    C B Hoyng
    0 references
    F P Cremers
    0 references
    April 1999
    0 references
    64
    0 references
    4
    0 references
    1024-35
    0 references

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit