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Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation

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Description scientific article
Author/s

author: Thomas Gasser  Elżbieta Jurkiewicz  Valeria Tiranti  Tomasz Kmieć  Juliane Winkelmann  Claudia Trenkwalder  Konrad Oexle  Maja Hempel  Sergiusz Jóźwiak  Thomas Klopstock  Małgorzata Krajewska-Walasek  Arcangela Iuso  Matthias Elstner  Sabrina Dusi  Tobias B Haack  Katharina Heim  Tim M Strom  Thomas Meitinger  Holger Prokisch  Gerd Schmitz 

Publication date October 1, 2011
Language English
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