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the identification genetic causes; a good example of this is work from Prof Hardy’s team on the discovery of the APP gene in Alzheimer’s disease (see review, J Neurochem. 2025 Jul;169(7):e70148. doi: 10.1111/jnc.70148
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PhD Studentship: Genetic modifiers to untangle disease mechanisms of RFC1 repeat expansion University College London � Queen Square Institute of Neurology Project: Biallelic repeat expansions in
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