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Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories - Arber - 2016 - Neuropathology and Applied Neurobiology - Wiley Online Library
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Frontiers | Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+
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Nazo, the Drosophila homolog of the NBIA-mutated protein – c19orf12, is required for triglyceride homeostasis | bioRxiv
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Frontiers | The Downregulation of c19orf12 Negatively Affects Neuronal and Musculature Development in Zebrafish Embryos
Alignment of the fly C19orf12 orthologs (CG3740, CG11671) with human... | Download Scientific Diagram
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Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation - ScienceDirect
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Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoform - ScienceDirect
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Frontiers | Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+
Brain iron and metabolic abnormalities in C19orf12 mutation carriers: A 7.0 tesla MRI study in mitochondrial membrane protein-associated neurodegeneration. - Munich Cluster for Systems Neurology - LMU Munich
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Frontiers | Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+
![PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/dd2ecb2012d86f9d3853c6aef367791e936d0787/11-Figure9-1.png)
PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar
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C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
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C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
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PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar
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