Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy. (Q45199881)

From Wikidata
Jump to navigation Jump to search
scientific article published in January 2004
edit
Language Label Description Also known as
English
Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy.
scientific article published in January 2004

    Statements

    Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy (English)

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit