« 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.
mars 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.