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RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions.
- Source :
- Neurology; 6/7/2011, Vol. 76 Issue 23, p2032-2034, 3p
- Publication Year :
- 2011
Details
- Language :
- English
- ISSN :
- 00283878
- Volume :
- 76
- Issue :
- 23
- Database :
- Supplemental Index
- Journal :
- Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 104806231
- Full Text :
- https://doi.org/10.1212/WNL.0b013e31821e558b