Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP). (Q46136658)

From Wikidata
Jump to navigation Jump to search
scientific article published in February 2009
edit
Language Label Description Also known as
English
Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP).
scientific article published in February 2009

    Statements

    Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP). (English)

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit