Cite
HARVARD Citation
Carrozzo, R. et al. (2016). Succinate‐CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. Journal of inherited metabolic disease. 39 (2), pp. 243-252. [Online].
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Carrozzo, R. et al. (2016). Succinate‐CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. Journal of inherited metabolic disease. 39 (2), pp. 243-252. [Online].