Author:
Martin J. -J.,Krols L.,Ceuterick C.,Van Broeckhoven C.,Van Regemorter N.,Hayer-Delatte F.,Brucher J. -M.,de Barsy T.,Szliwowski H.,Evrard P.,Tassignon M. -J.,Smet-Dieleman H.,Willems P. J.
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Reference33 articles.
1. Auburger G, Diaz GO, Capote RF, Sanchez SG, Perez MP, del Cueto ME, Meneses MG, Farrall M, Williamson R, Chamberlain S, Baute LH (1990) Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban Founder-effect population. Am J Hum Genet 46: 1163?1177
2. Bergstedt M, Johansson S, Müller R (1962) Hereditary spastic ataxia with central retinal degeneration and vestibular impairment. A clinical report on a family. Neurology 12: 124?132
3. Björk A, Lindblom U, Wadensten L (1956) Retinal degeneration in hereditary ataxia. J Neurol Neurosurg Psychiatry 19: 186?193
4. Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, von Gabain A, Farrall M, Williamson R (1988) Mapping of mutation causing Friedreich's ataxia to human chromosome 9. Nature 334: 248?250
5. Duinkerke-Eerola KU, Cruysberg JRM, Deutman AF (1980) Atrophic maculopathy associated with hereditary ataxia. Am J Ophthalmol 90: 597?603
Cited by
71 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献