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

J Neurol Sci

Institute of Neurological Sciences, National Research Council, Mangone, CS, Italy. Electronic address:

Published: January 2017

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http://dx.doi.org/10.1016/j.jns.2016.11.069	DOI Listing

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