1.
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
by Hartig, Monika B
American journal of human genetics, 2011, Vol.89 (4), p.543-550
2.
Absence of an orphan mitochondrial protein, C19orf12, causes a distinct clinical subtype of neurodegenration with brain iron accumulation
by Hartig, Monika B
American journal of human genetics, 2011, Vol.89 (4), p.543
