Ataxia with oculomotor apraxia type 2: Novel mutations in six patients with juvenile age of onset and elevated serum α-fetoprotein

Veronica Bernard^*, S. Stricker, F. Kreuz, M. Minnerop, G. Gillessen-Kaesbach, C. Zühlke

^*Corresponding author for this work

Institute of Human Genetics

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Cloning of the gene defect for spinocerebellar ataxia type 4 (SCA4)
Zühlke, C.
01.01.03 → 31.12.09
Project: DFG Projects › DFG Individual Projects