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PhD Studentship/Fellowship; Parkinson’s Disease, Spastic Paraplegia and Repeat Expansion Disorders: using Long-Read Sequencing to Identify Mechanisms and Disease Pathways

UCL | London, England | United Kingdom | about 2 hours ago

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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