Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
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Open Access
- 1 October 2011
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 89 (4), 543-550
- https://doi.org/10.1016/j.ajhg.2011.09.007
Abstract
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