Cohen-Barak E et al. A homozygote variant in CHMP3 is associated with complex hereditary spastic paraplegia. J Med Genet. 2022; PMID: 35710109.
CHMP3
Cohen-Barak E et al. A homozygote variant in CHMP3 is associated with complex hereditary spastic paraplegia. J Med Genet. 2022; PMID: 35710109.