Detection of Novel Mutations that Cause Autosomal Dominant Retinitis Pigmentosa in Candidate Genes
News Apr 09, 2013
Purpose of this study was to devise an effective method for detecting mutations in 12 genes commonly associated with autosomal dominant retinitis pigmentosa (adRP) that account for more than 95% of known mutations.
This study was published online in Molecular Vision and is free to access.
QIAGEN and CENTOGENE to Collaborate in Bioinformatics for Genetic DiseasesNews
Aiding the analysis of hereditary disorders by integrating genomic and clinical databases.READ MORE
Double Helix Technologies teams-up with Agilent TechnologiesNews
Collaboration will offer the SureVector cloning system for next-generation cloning.READ MORE