Cite
HARVARD Citation
Al‐Thihli, K. et al. (2021). Deficiency of acyl‐CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset. Clinical genetics. 99 (3), pp. 376-383. [Online].
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Al‐Thihli, K. et al. (2021). Deficiency of acyl‐CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset. Clinical genetics. 99 (3), pp. 376-383. [Online].