A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia | Journal of Medical Genetics

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Neurogenetics

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A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia

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Cite this article as:: Cohen-Barak E, Danial-Farran N, Chervinsky E, et al

A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia

Journal of Medical Genetics Published Online First: 16 June 2022. doi: 10.1136/jmedgenet-2022-108508