This article is part of a special issue on exome sequencing.
Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia
Genome Biology 2011, 12:R92 doi:10.1186/gb-2011-12-9-r92
- Last 30 days: 172 accesses
- Last 365 days: 1358 accesses
- All time: 6647 accesses
These numbers are accesses on BioMed Central websites only, and an underestimate of total usage. More information