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

Autor: McDermott CJ, Dayaratne RK, Tomkins J, Johnson MA, Turnbull DM, Bushby K, Shaw PJ, CASARI , GIORGIO NEVIO
Přispěvatelé: Mcdermott, Cj, Dayaratne, Rk, Tomkins, J, Johnson, Ma, Casari, GIORGIO NEVIO, Turnbull, Dm, Bushby, K, Shaw, Pj
Rok vydání: 2000
Databáze: OpenAIRE