Search Results - Neuser, Sonja

De novo variants in RAB11B cause various degrees of lobal developmental delay and intellectual disability in children by Ahmad, Natalie (Author) , Fazeli, Walid (Author) , Schließke, Sophia (Author) , Lesca, Gaetan (Author) , Gokce-Samar, Zeynep (Author) , Mekbib, Kedous Y. (Author) , Jin, Sheng Chih (Author) , Burton, Jennifer (Author) , Hoganson, George (Author) , Petersen, Andrea (Author) , Gracie, Sara (Author) , Granger, Leslie (Author) , Bartels, Enrika (Author) , Oppermann, Henry (Author) , Kundishora, Adam (Author) , Till, Marianne (Author) , Milleret-Pignot, Clara (Author) , Dangerfield, Shane (Author) , Viskochil, David (Author) , Anderson, Katherine J. (Author) , Palculict, Timothy Blake (Author) , Schnur, Rhonda E. (Author) , Wentzensen, Ingrid M. (Author) , Tiller, George E. (Author) , Kahle, Kristopher T. (Author) , Kunz, Wolfram S. (Author) , Burkart, Sebastian (Author) , Simons, Matias (Author) , Sticht, Heinrich (Author) , Abou Jamra, Rami (Author) , Neuser, Sonja (Author) ,

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• lizenzpflichtig

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15 by Saffari, Afshin (Author) , Kellner, Melanie (Author) , Jordan, Catherine (Author) , Rosengarten, Helena (Author) , Mo, Alisa (Author) , Zhang, Bo (Author) , Strelko, Oleksandr (Author) , Neuser, Sonja Anna (Author) , Davis, Marie Y (Author) , Yoshikura, Nobuaki (Author) , Futamura, Naonobu (Author) , Takeuchi, Tomoya (Author) , Nabatame, Shin (Author) , Ishiura, Hiroyuki (Author) , Tsuji, Shoji (Author) , Aldeen, Huda Shujaa (Author) , Cali, Elisa (Author) , Rocca, Clarissa (Author) , Houlden, Henry (Author) , Efthymiou, Stephanie (Author) , Assmann, Birgit (Author) , Yoon, Grace (Author) , Trombetta, Bianca A (Author) , Kivisäkk, Pia (Author) , Eichler, Florian (Author) , Nan, Haitian (Author) , Takiyama, Yoshihisa (Author) , Tessa, Alessandra (Author) , Santorelli, Filippo M (Author) , Sahin, Mustafa (Author) , Blackstone, Craig (Author) , Yang, Edward (Author) , Schüle-Freyer, Rebecca (Author) , Ebrahimi-Fakhari, Darius (Author) ,

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Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies by Schröter, Julian (Author) , Popp, Bernt (Author) , Brennenstuhl, Heiko (Author) , Driedger, Jan Henje (Author) , Jestaedt, Leonie (Author) , Arélin, Maria (Author) , Gräfe, Daniel (Author) , Neuser, Sonja Anna (Author) , Parker, Michael (Author) , Lemke, Johannes (Author) , Hoffmann, Georg F. (Author) , Kölker, Stefan (Author) , Harting, Inga (Author) , Syrbe, Steffen (Author) ,

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• kostenfrei