Cite
HARVARD Citation
Riley, L. et al. (2017). A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders. Journal of inherited metabolic disease. 40 (2), pp. 261-269. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Riley, L. et al. (2017). A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders. Journal of inherited metabolic disease. 40 (2), pp. 261-269. [Online].