Corrigendum to “The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation.” Clin Chim Acta, volume 436, pages 135–139

詳細情報 詳細情報について

• CRID

  1870302167910736384

• DOI

  10.1016/j.cca.2015.04.001

• ISSN

  00098981

• データソース種別

  • OpenAIRE