Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1.

Author:

Jobsis G J,Weber J W,Barth P G,Keizers H,Baas F,van Schooneveld M J,van Hilten J J,Troost D,Geesink H H,Bolhuis P A

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference19 articles.

1. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias;Harding, A.E.;Brain,1982

2. Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: a clinical and genetic study of eight families;Enevoldson, T.P.; Sanders, M.D.; Harding, A.E.;Brain,1994

3. Autosomal dominant cerebellar phenotypes: the genotype has settled the issue;Rosenberg, R.N.;Neurology,1995

4. A third locus for autosomal dominant cerebellar ataxia type 1 maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus;Stevanin, G.; LeGuem, E.; Ravise, N.;Am J Hum Genet,1994

5. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11;Ranum, L.P.W.; Schut, L.J.; Lundgren, J.K.; Orr, H.T.; Livingston, D.M.;Nature Genet,1994

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