Search All UT System Experts

A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions

Henna Tyynismaa, Emil Ylikallio, Mehul Patel, Maria J. Molnar, Ronald G. Haller, Anu Suomalainen

Research output: Contribution to journal › Article › peer-review

105 Scopus citations

Fingerprint

Dive into the research topics of 'A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions'. Together they form a unique fingerprint.

Medicine & Life Sciences