FMR1 premutation as a rare cause of late onset ataxia--evidence for FXTAS in female carriers von Zühlke, Ch, Budnik, A, Gehlken, U, Dalski, A, Purmann, S, Naumann, M, Schmidt, M, Bürk, K, Schwinger, E

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SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6 von ZÜHLKE, C. H, SPRANGER, M, SPRANGER, S, VOIGT, R, LANZ, M, GEHLKEN, U, HINRICHS, F, SCHWINGER, E

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Phenotypical variability of expanded alleles in the TATA-binding protein gene: Reduced penetrance in SCA17? von ZÜHLKE, Christine, GEHLKEN, Ulrike, HELLENBROICH, Yorck, SCHWINGER, Eberhard, BÜRK, Katrin

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CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 alleles von ZÜHLKE, C, HELLENBROICH, Y, SCHAAFF, F, GEHLKEN, U, WESSEL, K, SCHUBERT, T, CERVOS-NAVARRO, J, PICKARTZ, H, SCHWINGER, E

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Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families von Zühlke, Christine, Gehlken, Ulrike, Purmann, Sabine, Kunisch, Markus, Müller-Myhsok, Bertram, Kreuz, Friedmar, Laccone, Franco

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