Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol
Titel:
Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol
Auteur:
Lobitz, Stephan Frömmel, Claudia Brose, Annemarie Blankenstein, Oliver Turner, Charles Dalton, R. Neil Daniel, Yvonne Klein, Jeannette