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Maternal Carnitine Uptake Defect (mCUD) and S467C While we performed mutation analysis for NBS screen-positive CUD neonates referred from Taiwan screening centres, there were occasional newborns with whom only one mutation was found
doi: 10.1096/fj.07-9239com 106 NakshabendiI
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[Google Scholar] 5.Caspi A, Sugden K, Moffitt TE, Taylor A, Craig IW, Harrington H, et al
