MeSH Browser

MeSH Supplementary: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Unique ID: C563747
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563747
Entry Term(s): Progressive External Ophthalmoplegia, Autosomal Dominant, 3
Registry Number: 0
Heading Mapped to: *Ophthalmoplegia, Chronic Progressive External
Frequency: 0
Note: mutation in twinkle gene
Date of Entry: 2012/11/05

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 MeSH Supplementary Concept Data 2024