Finding the needle in a genomic haystack

Friday, February 3, 2017 - 16:01 in Biology & Nature

Researchers have identified a genomic mutation that causes physical abnormalities and developmental delays in children. Upon analyzing the genome of a six-year-old boy, the scientists identified a novel mutation that affects a protein known as CASK, which is key to brain development and the signals transmitted by brain cells, or neurons.

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