Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder (Q56552029)

From Wikidata
Jump to navigation Jump to search
article published in 2001
edit
Language Label Description Also known as
English
Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder
article published in 2001

    Statements

    Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder (English)
    0 references
    M. Lebel
    0 references
    1 June 2001
    0 references
    58
    0 references
    857-867
    0 references
    7
    0 references

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit