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This is a citation of an outside article. Gravyday is not responsible for its content. Original URL below.

CRISPR fixes disease gene in viable human embryos
Gene-editing experiment pushes scientific and ethical boundaries.
An international team of researchers has used CRISPR–Cas9 gene editing — a technique that allows scientists to make precise changes to genomes with relative ease — to correct a disease-causing mutation in dozens of viable human embryos. The study represents a significant improvement in efficiency and accuracy over previous efforts.(more)

Reported By: www.nature.com