MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion. (Q43196100)

From Wikidata
Jump to navigation Jump to search
scientific article published on 31 December 2009
edit
Language Label Description Also known as
English
MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion.
scientific article published on 31 December 2009

    Statements

    MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion (English)

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit