Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol.
作者信息
Lobitz Stephan, Frömmel Claudia, Brose Annemarie, Blankenstein Oliver, Turner Charles, Dalton R Neil, Daniel Yvonne, Klein Jeannette
机构信息
Department of Pediatric Hematology and Oncology, Gemeinschaftsklinikum Mittelrhein, Koblenzer Strasse 115-155, 56073, Koblenz, Germany.
Department of Laboratory Medicine, Alexianer St. Hedwig Krankenhaus, Berlin, Germany.
出版信息
Ann Hematol. 2022 Aug;101(8):1859-1860. doi: 10.1007/s00277-022-04811-0. Epub 2022 Mar 16.
PMID:35293609
Abstract
摘要
Zotero 插件