Author:
Gispert S.,Twells R.,Orozco G.,Brice A.,Weber J.,Heredero L.,Scheufler K.,Riley B.,Allotey R.,Nothers C.,Hillermann R.,Lunkes A.,Khati C.,Stevanin G.,Hernandez A.,Magariño C.,Klockgether T.,Durr A.,Chneiweiss H.,Enczmann J.,Farrall M.,Beckmann J.,Mullan M.,Wernet P.,Agid Y.,Freund H.-J.,Williamson R.,Auburger G.,Chamberlain S.
Publisher
Springer Science and Business Media LLC
Reference23 articles.
1. Weatherall, D.J. The New Genetics and Clinical Practice (Oxford University Press, Oxford 1984).
2. Pogacar, S. et al. Dominant spino–pontine atrophy: Report of two additional members of the family W. Arch. Neurol. 35, 156–162 (1978).
3. Brown, S. On hereditary ataxy, with a series of twenty-one cases. Brain 15, 250–268 (1982).
4. Konigsmark, B.W. & Lipton, H.L. Dominant olivo–ponto–cerebellar atrophy with extrapyramidal signs. Report of a family through three generations. Birth Defects Orig. Art. Ser. 1, 178–191 (1971).
5. Weiner, L.P., Konigsmark, B.W., Stoll, J. Jr. & Magladery, J.W. Hereditary olivo–ponto–cerebellar atrophy with retinal degeneration. Report of a family through six generations. Arch. Neurol. 16, 364–376 (1967).
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