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30. The rare and the common: An Austrian DRPLA family harboring the European haplotype. Amprosi M; Zech M; Lichtner P; Eckstein G; Unterberger I; Eigentler A; Indelicato E; Puttinger G; Nachbauer W; Boesch S Parkinsonism Relat Disord; 2021 Jun; 87():119-121. PubMed ID: 34022586 [TBL] [Abstract][Full Text] [Related]
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33. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530 [TBL] [Abstract][Full Text] [Related]
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