Authors: Hartig, Monika B. Iuso, Arcangela Haack, Tobias Kmiec, Tomasz

Citation: B. Hartig, Monika et al., Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation, American journal of human genetics (Online) AJHG , 89(4), 2011, pp. 543-550