Cite
HARVARD Citation
Reid, E. et al. (2017). Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Journal of inherited metabolic disease. 40 (3), pp. 385-394. [Online].
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Reid, E. et al. (2017). Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Journal of inherited metabolic disease. 40 (3), pp. 385-394. [Online].