Copeland,William C

Institution: National Institutes of Health, USA

Top Collaborators: Kasiviswanathan R, Stumpf JD, Longley MJ, Young MJ, Humble MM, Pandiri AR, Travlos GS, Chan SS, Foley JF, Minko IG, Naviaux RK, Lloyd RS, Basinger AA, Saneto RP, Casas KA, Bailey CM, Spell D, Stillwagon M, Anderson KS, Sharief FS

Research Interests: DNA, Mitochondrial DNA, Mutations, Disease, Gene, Mtdna, Human, Syndrome, Diseases, Ataxia, External Ophthalmoplegia, Ophthalmoplegia, Progressive External Ophthalmoplegia, Enzymes, Phenotype, Alpers Syndrome, Mitochondrial Disease, Catalytic Subunit, Point Mutations, Mitochondrial Diseases