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C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis

Marcus Deschauer, Charly Gaul, Curd Behrmann, Holger Prokisch, S. Zierz, Tobias B. Haack

Journal of Neurology · 2012 · 64 citations · 1 references

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References

1

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Monika Hartig, Arcangela Iuso, Tobias B. Haack et al. · The American Journal of Human Genetics · 2011 · 266 citations · Full text

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