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

mutation in POLG

Date introduced: November 5, 2012

MeSH Unique ID: C564926

Heading Mapped to:

• Ophthalmoplegia

Entry Terms:

• Progressive External Ophthalmoplegia, Autosomal Recessive