Cite
HARVARD Citation
Shafqat, N. et al. (2013). A structural mapping of mutations causing succinyl‐CoA:3‐ketoacid CoA transferase (SCOT) deficiency. Journal of inherited metabolic disease. 36 (6), pp. 983-987. [Online].
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Shafqat, N. et al. (2013). A structural mapping of mutations causing succinyl‐CoA:3‐ketoacid CoA transferase (SCOT) deficiency. Journal of inherited metabolic disease. 36 (6), pp. 983-987. [Online].