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Shortland G, Besley G, Bonham J, et al (2006) Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency (MCADD): findings from a multicentre prospective UK collaborative study. J Inherit Metab Dis 29(Supplement 1): 19.
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Competing interests: On behalf of UKCSNS-MCADD. The UKCSNS-MCADD was funded by a grant from the UK Department of Health and the National Screening Committee.
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Downing, M., Manning, N.J., Dalton, R.N. et al. Detection of urinary hexanoylglycine in the diagnosis of MCAD deficiency from newborn screening. J Inherit Metab Dis 31, 550 (2008). https://doi.org/10.1007/s10545-008-9976-z
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DOI: https://doi.org/10.1007/s10545-008-9976-z