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SPG43 and ALS-like syndrome in the same family due to compound heterozygous mutations of the C19orf12 gene: a case description and brief review | SpringerLink
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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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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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C19orf12 ablation causes ferroptosis in mitochondrial membrane protein-associated with neurodegeneration - ScienceDirect
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Neurodegeneration of diPLA2-VIA −/− flies is rescued by MPAN-associated... | Download Scientific Diagram
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Frontiers | The Downregulation of c19orf12 Negatively Affects Neuronal and Musculature Development in Zebrafish Embryos
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Frontiers | Case Report: Identification of a De novo C19orf12 Variant in a Patient With Mitochondrial Membrane Protein–Associated Neurodegeneration
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C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
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Pharmaceutics | Free Full-Text | Identification of Autophagy as a Functional Target Suitable for the Pharmacological Treatment of Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN) In Vitro
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C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
![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/dd2ecb2012d86f9d3853c6aef367791e936d0787/5-Figure1-1.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
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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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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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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Pharmaceuticals | Free Full-Text | Neurodegeneration with Brain Iron Accumulation Disorders: Valuable Models Aimed at Understanding the Pathogenesis of Iron Deposition
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