![Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2020/03/04/2020.03.02.973909/F1.large.jpg)
Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv
![Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies | Scientific Reports Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41598-017-00208-6/MediaObjects/41598_2017_208_Fig1_HTML.jpg)
Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies | Scientific Reports
![Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2020/03/04/2020.03.02.973909/F5.large.jpg)
Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv
![Frontiers | Functional Genomics of PRUNE1 in Neurodevelopmental Disorders (NDDs) Tied to Medulloblastoma (MB) and Other Tumors Frontiers | Functional Genomics of PRUNE1 in Neurodevelopmental Disorders (NDDs) Tied to Medulloblastoma (MB) and Other Tumors](https://www.frontiersin.org/files/Articles/758146/fonc-11-758146-HTML/image_m/fonc-11-758146-g001.jpg)
Frontiers | Functional Genomics of PRUNE1 in Neurodevelopmental Disorders (NDDs) Tied to Medulloblastoma (MB) and Other Tumors
![Mitochondrial Superoxide Dismutase: What the Established, the Intriguing, and the Novel Reveal About a Key Cellular Redox Switch | Antioxidants & Redox Signaling Mitochondrial Superoxide Dismutase: What the Established, the Intriguing, and the Novel Reveal About a Key Cellular Redox Switch | Antioxidants & Redox Signaling](https://www.liebertpub.com/cms/10.1089/ars.2019.7962/asset/images/medium/ars.2019.7962_figure1.jpg)
Mitochondrial Superoxide Dismutase: What the Established, the Intriguing, and the Novel Reveal About a Key Cellular Redox Switch | Antioxidants & Redox Signaling
![An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families - Koko - 2021 - Annals of Human Genetics - Wiley Online Library An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families - Koko - 2021 - Annals of Human Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/80a50a7b-4cd3-4722-927e-da29aa2687a4/ahg.v85.5.cover.jpg?trick=1692707460271)
An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families - Koko - 2021 - Annals of Human Genetics - Wiley Online Library
![Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2020/03/04/2020.03.02.973909/F13.large.jpg)
Functional modeling of NMIHBA-causing PRUNE1 variants reveals a requirement for its exopolyphosphatase activity | bioRxiv
![Mitochondrial Superoxide Dismutase: What the Established, the Intriguing, and the Novel Reveal About a Key Cellular Redox Switch | Antioxidants & Redox Signaling Mitochondrial Superoxide Dismutase: What the Established, the Intriguing, and the Novel Reveal About a Key Cellular Redox Switch | Antioxidants & Redox Signaling](https://www.liebertpub.com/cms/10.1089/ars.2019.7962/asset/images/medium/ars.2019.7962_figure3.jpg)