Direct Detection of Low Abundance Genes of Single Point Mutation | Nano Letters
Human ARHGEF9 intellectual disability syndrome is phenocopied by a mutation that disrupts collybistin binding to the GABAA receptor α2 subunit | Molecular Psychiatry
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Circulating tumour DNA analysis to direct therapy in advanced breast cancer (plasmaMATCH): a multicentre, multicohort, phase 2a, platform trial - The Lancet Oncology
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Rare genetic mutation leaves people at higher risk for multiple cancers | Penn Today
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The Quantum Human: Understanding the Evolution of Consciousness, the Solar Plexus Mutation, and Human Design - Publishing for Thought Leaders and Experts
Cancer gene mutation frequencies for the U.S. population | Nature Communications
Cardiac genetic mutation may not always predict heart disease | Penn Today