Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.
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Authors
Knottnerus, Suzan J GPras-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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ArticleLanguage
en
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Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.Published in
Biochim Biophys Acta Mol Basis Dis 2020; 1866(6):165725PMID
32061778ae974a485f413a2113503eed53cd6c53
10.1016/j.bbadis.2020.165725
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