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5. Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care

6. The M1311V variant of ATP7A is associated with impaired trafficking and copper homeostasis in models of motor neuron disease

10. Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36

22. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis

26. Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo

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