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  1. Rautenberg, Katrin [Editor] ; Brandenburg Landesrechnungshof, Mecklenburg-Vorpommern Landesrechnungshof, Sachsen Sächsischer Rechnungshof, Landesrechnungshof Sachsen-Anhalt, Thüringen Rechnungshof

    Fünfundzwanzig Jahre Rechnungshöfe der neuen Bundesländer : Jubiläumsschrift

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    [Erscheinungsort nicht ermittelbar]: [Verlag nicht ermittelbar], 2016

    Saxon Bibliography (Sächsische Bibliografie)
  3. Gericke, Katrin [Author]; Rautenberg, Brit [Author]; Sprengel, Hans-Jürgen [Author] ; Pädagogische Hochschule Karl Liebknecht

    Mathematische außerunterrichtliche Tätigkeit in der Unterstufe (Klasse 3) : Theorie und Praxis

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    Potsdam: Rektor d. Pädag. Hochsch. Karl Liebknecht, 1987

    Published in: Pädagogische Hochschule Karl Liebknecht: Potsdamer Forschungen der Pädagogischen Hochschule "Karl Liebknecht" / C ; 7100

  5. Park, Joohyun; Flores, Bianca R; Scherer, Katalin; Kuepper, Hanna; Rossi, Mari; Rupprich, Katrin; Rautenberg, Maren; Deininger, Natalie; Weichselbaum, Annette; Grimm, Alexander; Sturm, Marc; Grasshoff, Ute; Delpire, Eric; Haack, Tobias B

    De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy

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    BMJ, 2020

    Published in: Journal of Medical Genetics

  6. Van de Vondel, Liedewei; De Winter, Jonathan; Beijer, Danique; Coarelli, Giulia; Wayand, Melanie; Palvadeau, Robin; Pauly, Martje G.; Klein, Katrin; Rautenberg, Maren; Guillot‐Noël, Léna; Deconinck, Tine; Vural, Atay; Ertan, Sibel; Dogu, Okan; Uysal, Hilmi; Brankovic, Vesna; Herzog, Rebecca; Brice, Alexis; Durr, Alexandra; Klebe, Stephan; Stock, Friedrich; Bischoff, Almut Turid; Rattay, Tim W.; Sobrido, María‐Jesús; [...]

    De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia

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    Wiley, 2022

    Published in: Movement Disorders

  7. Park, Joohyun; Tucci, Arianna; Cipriani, Valentina; Demidov, German; Rocca, Clarissa; Senderek, Jan; Butryn, Michaela; Velic, Ana; Lam, Tanya; Galanaki, Evangelia; Cali, Elisa; Vestito, Letizia; Maroofian, Reza; Deininger, Natalie; Rautenberg, Maren; Admard, Jakob; Hahn, Gesa-Astrid; Bartels, Claudius; van Os, Nienke J.H.; Horvath, Rita; Chinnery, Patrick F.; Tiet, May Yung; Hewamadduma, Channa; Hadjivassiliou, Marios; [...]

    Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy

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    Elsevier BV, 2022

    Published in: Genetics in Medicine