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OPA3
Neurologic Outcomes in Friedreich Ataxia: Study of a Single-Site Cohort E415
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Mitochondrial Localization and Ocular Expression of Mutant Opa3 in a Mouse Model of 3-Methylglutaconicaciduria Type III
Association Analyses of 249,796 Individuals Reveal 18 New Loci
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Powerful Gene-Based Testing by Integrating Long-Range Chromatin Interactions and Knockoff Genotypes
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
3-Methylglutaconic Aciduria Type III in a Non-Iraqi-Jewish Kindred: Clinical and Molecular findings
A Third Locus for Dominant Optic Atrophy on Chromosome
Nuclear and Mitochondrial Analysis of Patients with Primary Angle-Closure Glaucoma
Correspondence on Lovell Et Al.: Identification of Chicken Genes Previously Assumed to Be Evolutionarily Lost
Rapid Phenotype-Driven Gene Prioritization for Rare Diseases
HBV DNA Integration and Clonal Hepatocyte Expansion in Chronic Hepatitis B Patients Considered Immune Tolerant
Genetic Screening for OPA1 and OPA3 Mutations in Patients With
Genome-Wide Association Study of Comorbid Depressive Syndrome and Alcohol Dependence Alexis C
OPA3 Gene OPA3, Outer Mitochondrial Membrane Lipid Metabolism Regulator
CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria
Molecular Characterization of Familial Ataxic, Paraplegic and Related Movement Disorders
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