(Q44120180)

English

A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients

scientific article published in September 2002

Statements

A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients (English)
1 September 2002

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit