Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 [Supplementary Concept]

mutation in twinkle gene

Date introduced: November 5, 2012

MeSH Unique ID: C563747

Heading Mapped to:

• Ophthalmoplegia, Chronic Progressive External

Entry Terms:

• Progressive External Ophthalmoplegia, Autosomal Dominant, 3