36BD052D-0F65-4CE8-BA67-339C04BF3CFDExome sequencing in motor neuron disease: bioinformatic analyses and biological validation of novel variantsResearch GrantMR/L021803/1C008C651-F5B0-4859-A334-5F574AB6B57CMRCINCOME_ACTUAL7295427846F5BF-DE90-46B5-A264-D15686F66468VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.Journal of the neurological sciences4ca9888509a2e1aa2bdbb5ae3b44a8e0Kwok CT2015-01-01http://dx.doi.org/10.1016/j.jns.2015.01.02125618255http://ukpmc.ac.uk/abstract/MED/256182550022-510Xhttp://europepmc.org/abstract/MED/256182553491-2Journal Article/Reviewdoi_55f9859851a8bffe