Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments

Magariello, A., Russo, C., Citrigno, L., Züchner, S., Patitucci, A., Mazzei, R., … Muglia, M. (2017, January 15). Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments. Journal of the Neurological Sciences. Elsevier B.V. https://doi.org/10.1016/j.jns.2016.11.069