TY  - CONF

T1  - Hereditary spastic paraparesis with amyotrophy and OXPHOS muscle defect associated with a deletion in the paraplegin (SPG7) gene with apparent autosomal dominant transmission

JO  - NEUROLOGY

PY  - 2000/04/11

AU  - McDermott CJ

AU  - Dayaratne RK

AU  - Tomkins J

AU  - Johnson MA

AU  - Casari G

AU  - Turnbull DM

AU  - Bushby K

AU  - Shaw PJ

ED  - 

VL  - 54

IS  - 7

SP  - A425

EP  - A425

Y2  - 2024/12/22

ER  -