Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations
A. Benomar, F. Meggouh, O. Didierjean, N. Kissani, A. Dürr, A. Sefiani, T. Chkili, Y. Agid, M. Yahyaoui, A. BriceVolume:
3
Year:
1996
Language:
english
Pages:
4
DOI:
10.1111/j.1468-1331.1996.tb00231.x
File:
PDF, 256 KB
english, 1996