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HARVARD Citation
Cohen-Barak, E. et al. (2023). A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia. Journal of medical genetics. 60 (3), pp. 233-240. [Online].
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Cohen-Barak, E. et al. (2023). A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia. Journal of medical genetics. 60 (3), pp. 233-240. [Online].