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    Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.

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    Authors
    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
    Type
    Article
    Language
    en
    
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    Title
    Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.
    Published in
    Biochim Biophys Acta Mol Basis Dis 2020; 1866(6):165725
    DOI
    10.1016/j.bbadis.2020.165725
    PMID
    32061778
    URI
    http://hdl.handle.net/10029/623771
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.bbadis.2020.165725
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