(Q37693980)

English

Mechanisms of disease and clinical features of mutations of the gene for mitofusin 2: an important cause of hereditary peripheral neuropathy with striking clinical variability in children and adults

scientific article published on 12 February 2010

Statements

Mechanisms of disease and clinical features of mutations of the gene for mitofusin 2: an important cause of hereditary peripheral neuropathy with striking clinical variability in children and adults (English)
12 February 2010
328-330

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit