TY - CONF T1 - Mutations in SPG7 as an important cause of spastic-ataxia in a large british cohort: Hybrid phenotype helps direct screening JO - Journal of the Neurological Sciences UR - http://eprints.whiterose.ac.uk/129741/ PY - 2017/10/15 AU - Hewamadduma CA AU - Omalley R AU - Robinson M AU - Beauchamp N AU - Rogers T AU - Martindale J AU - Mcdermott C AU - Shaw P AU - Hoggard N AU - Hadjivassiliou M ED - DO - DOI: 10.1016/j.jns.2017.08.864 PB - Elsevier VL - 381 SP - 304 EP - 305 Y2 - 2025/04/12 ER -