Søgeresultater - Andrew Wilber
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Maternal Primary Carnitine Deficiency and a Novel Solute Carrier Family 22 Member 5 (SLC22A5) Mutation af Michael Jakoby MD, MA, Amruta Jaju MD, Aundrea Marsh BS, Andrew Wilber PhD
Udgivet 2021Klassifikationsnummer: Loading...Connect to this object online.
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Efficient Non-Viral Integration and Stable Gene Expression in Multipotent Adult Progenitor Cells af Andrew Wilber, Fernando Ulloa Montoya, Luke Hammer, Branden S. Moriarity, Aron M. Geurts, David A. Largaespada, Catherine M. Verfaillie, R. Scott McIvor, Uma Lakshmipathy
Udgivet 2011Klassifikationsnummer: Loading...Connect to this object online.
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