Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion (Q33625619)

From Wikidata
Jump to navigation Jump to search
scientific article
edit
Language Label Description Also known as
English
Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion
scientific article

    Statements

    Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion (English)
    Michael W Lawlor
    Elizabeth T Dechene
    Amelia S Geggel
    Behzad Moghadaszadeh
    Alan H Beggs
    1 February 2010

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit