Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia (Q36535853)

From Wikidata
Jump to navigation Jump to search
scientific article published on 17 September 2012
edit
Language Label Description Also known as
English
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
scientific article published on 17 September 2012

    Statements

    Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia (English)
    0 references
    0 references
    Lijia Huang
    Melissa T Carter
    Kathie L Friend
    Tracy E Dudding
    Ruobing Zou
    Peter W Schofield
    Stuart Douglas
    Dennis E Bulman
    17 September 2012

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit