„ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia” has been published in Neurology Genetics. This work was supported in part by JPND through 3DPD, selected in the 2015 JPco-fuND call.
martie 27, 2018
„ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia” has been published in Neurology Genetics. This work was supported in part by JPND through 3DPD, selected in the 2015 JPco-fuND call.