ALL libraries (COBIB.SI union bibliographic/catalogue database)
PDF
  • The C9ORF72 expansion mutation is a common cause of ALS + l-FTD in Europe and has a single founder
    Smith, Bradley N. ...
    Source: EJHG. European journal of human genetics. - ISSN 1018-4813 (Vol. 21, issue 1, 2013, str. 102-108)
    Type of material - article, component part
    Publish date - 2013
    Language - english
    COBISS.SI-ID - 26001703
    DOI

Shelf entry