Back to Search
Start Over
Two novel RRM2B gene mutations in a patient with autosomal recessive progressive external ophthalmoplegia, encephalopathy and cytochrome c oxidase deficiency
- Source :
- Mitochondrion. 12:562-563
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
Details
- ISSN :
- 15677249
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Mitochondrion
- Accession number :
- edsair.doi...........7071967d69413281ab9f912018199441