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Autor:
R M, Castilhos, A F D, Souza, G V, Furtado, T C, Gheno, A L, Silva, F R, Vargas, M-A F D, Lima, O, Barsottini, J L, Pedroso, C, Godeiro, D, Salarini, E T, Pereira, K, Lin, M-B, Toralles, J A M, Saute, C R, Rieder, M, Quintas, J, Sequeiros, I, Alonso, M L, Saraiva-Pereira, L B, Jardim
Publikováno v:
Clinical genetics. 86(4)
The aim of this study was to identify the relative frequency of Huntington's disease (HD) and HD-like (HDL) disorders HDL1, HDL2, spinocerebellar ataxia type 2 (SCA2), SCA17, dentatorubral-pallidoluysian degeneration (DRPLA), benign hereditary chorea