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    High-throughput genetic newborn screening for spinal muscular atrophy by rapid nucleic acid extraction from dried blood spots and 384-well qPCR

    High-throughput genetic newborn screening for spinal muscular atrophy by rapid nucleic acid extraction from dried blood spots and 384-well qPCR 由 Ludwig Czibere, Siegfried Burggraf, Tobias Fleige, Birgit Glück, Lisa Marie Keitel, Olfert Landt, Jürgen Durner, Wulf Röschinger, Katharina Hohenfellner, Brunhilde Wirth, Wolfgang Müller‐Felber, Katharina Vill, Marc Becker

    出版 2019
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