Genome-Wide Studies to Identify Rare Variants in BAG3
|June 30, 2011|
|6:00 pm||to||7:00 pm|
The June webinar of the free NimbleGen webinar series is talking about
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy >
For further information and registration, please visit the NimbleGen website.