New high throughput sequencing technology to identify genetic defects in rare diseases
The majority of rare diseases are hereditary. But despite significant progress in genome research, in most cases their exact cause remains unclear. The discovery of the underlying genetic defect is, however, a prerequisite for their definitive diagnosis and the development of innovative approaches to their treatment. Scientists at the Max Planck Institute for Molecular Genetics and the Institute …
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TRIALS WITHOUT TRIBULATIONS AMA National champion, locals show their stuff in Ottawa trials event
OTTAWA — Deep in the woods off Route 6, Patrick Smage eyed a rock cliff and studied it intently, his motorcycle at his side. After a few minutes, he heated up the motor and then took off, riding directly
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