Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots
| Autor: | Knottnerus, Suzan J.G., Pras-Raves, Mia L., van der Ham, Maria, Ferdinandusse, Sacha, Houtkooper, Riekelt H., Schielen, Peter C.J.I., Visser, Gepke, Wijburg, Frits A., de Sain-van der Velden, Monique G.M. |
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| Zdroj: | In BBA - Molecular Basis of Disease 1 June 2020 1866(6) |
| Databáze: | ScienceDirect |
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