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 |
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Přispěvatelé: | Mcdermott, Cj, Dayaratne, Rk, Tomkins, J, Johnson, Ma, Casari, GIORGIO NEVIO, Turnbull, Dm, Bushby, K, Shaw, Pj |
Rok vydání: | 2000 |
Databáze: | OpenAIRE |
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