A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions (Q37301264)
Jump to navigation
Jump to search
scientific article published on 06 August 2009
Language | Label | Description | Also known as |
---|---|---|---|
English | A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions |
scientific article published on 06 August 2009 |
Statements
1 reference
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions (English)
1 reference
Mehul Patel
1 reference
Maria J Molnar
1 reference
Ronald G Haller
1 reference
Anu Suomalainen
1 reference
6 August 2009
1 reference
1 reference
290-295
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference