Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [Supplementary Concept]
aka PEOA5; mutations in RRM2B
Date introduced: August 24, 2012
MeSH Unique ID: C567768
Heading Mapped to:
Entry Terms:
- Peoa5
- Progressive External Ophthalmoplegia, Autosomal Dominant, 5