Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3

Any autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the TK2 gene.

Also known as: PEOB3, TK2 autosomal recessive progressive external ophthalmoplegia, autosomal recessive progressive external ophthalmoplegia caused by mutation in TK2, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3; PEOB3, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 3, progressive external ophthalmoplegia, autosomal recessive 3

19 clinical trials for this condition and its sub-types.