Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy (Q48255402)

From Wikidata
Jump to navigation Jump to search
scientific article published on 30 March 2015
edit
Language Label Description Also known as
English
Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy
scientific article published on 30 March 2015

    Statements

    Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy (English)

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit