Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin (Q44706163)

From Wikidata
Jump to navigation Jump to search
scientific article published in January 2004
edit
Language Label Description Also known as
English
Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin
scientific article published in January 2004

    Statements

    Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin (English)
    Reidunn C J Bekkeheien
    Naomi Fukai
    Eileen Boye
    Gyorgy Kosztolanyi
    Salim Aftimos
    Samuel Deutsch
    Bjorn R Olsen
    1 January 2004

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit