A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Riley, Lisa G.
Cowley, Mark J.
Thorburn, David R.
Sue, Carolyn M.
Funding for this research was provided by:
National Health and Medical Research Council (APP1008433, 1026891)
New South Wales Office of Health and Medical Research
unspecified valid from 2016-12-19