Gene Expression Analyses Identify Narp Contribution in the Development of l-DOPA-Induced Dyskinesia | Journal of Neuroscience
A schematic of the novel strategy for gene therapy of NARP disease... | Download Scientific Diagram
Part:BBa K3411020 - parts.igem.org
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome | Neurology Genetics
Pentraxin - an overview | ScienceDirect Topics
Part:BBa K3411020 - parts.igem.org
Frontiers | The Role of Neuronal Pentraxin 2 (NP2) in Regulating Glutamatergic Signaling and Neuropathology
Frontiers | Non-Cell-Autonomous Factors Implicated in Parvalbumin Interneuron Maturation and Critical Periods
Part:BBa K3411020 - parts.igem.org
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein | Journal of Medical Genetics
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
Neuropathy, Ataxia and Retinitis Pigmentosa (NARP Syndrome)
IJMS | Free Full-Text | Mitochondrial Retinopathies
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
The neurology of mitochondrial DNA disease - The Lancet Neurology
Neuropathy, ataxia, and retinitis pigmentosa - Wikipedia
Frontiers | Mitochondrial Medicine: Genetic Underpinnings and Disease Modeling Using Induced Pluripotent Stem Cell Technology
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein | Journal of Medical Genetics
Narp Is Downstream of BDNF Signaling (A and B) Expression of Narp in... | Download Scientific Diagram
Sustained Increase in Narp Protein Expression Following Repeated Electroconvulsive Seizure | Neuropsychopharmacology
A schematic of the novel strategy for gene therapy of NARP disease... | Download Scientific Diagram
Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome | Neurology Genetics
