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Updated: Oct 6, 2025

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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A novel homozygous mutation in TBK1 gene causing ALS-FTD
Laura Libonati1, Marco Ceccanti2, Chiara Cambieri2
1Rare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy. laura.libonati@uniroma1.it.
Summary
No abstract available in PubMed .
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