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  - 2024/12/22

ER  -