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Zeitschriftenartikel
Al‐Azzani, Mohammed 
ORCID: https://orcid.org/0000-0003-2864-0854; Weber, Sandrina ORCID: https://orcid.org/0000-0001-5713-2141; Ramalingam, Nagendran ORCID: https://orcid.org/0000-0002-9459-3593; Ramón, Maria; Shvachiy, Liana; Mestre, Gonçalo; Zech, Michael ORCID: https://orcid.org/0000-0001-8112-9153; Sicking, Kevin; de Opakua, Alain Ibáñez; Jayanthi, Vidyashree; Amaral, Leslie; Agarwal, Aishwarya; Chandran, Aswathy; Chaves, Susana R.; Winkelmann, Juliane; Trenkwalder, Claudia; Schwager, Maike; Pauli, Silke; Dettmer, Ulf; Fernández, Claudio O.; Lautenschläger, Janin; Zweckstetter, Markus; Fernandez‐Busnadiego, Ruben; Mollenhauer, Brit ORCID: https://orcid.org/0000-0001-8437-3645 und Outeiro, Tiago Fleming
(2025):
A Novel α‐Synuclein K58N Missense Variant in a Patient with Parkinson's Disease.
In: Movement Disorders
ORCID: https://orcid.org/0000-0003-2864-0854; Weber, Sandrina ORCID: https://orcid.org/0000-0001-5713-2141; Ramalingam, Nagendran ORCID: https://orcid.org/0000-0002-9459-3593; Ramón, Maria; Shvachiy, Liana; Mestre, Gonçalo; Zech, Michael ORCID: https://orcid.org/0000-0001-8112-9153; Sicking, Kevin; de Opakua, Alain Ibáñez; Jayanthi, Vidyashree; Amaral, Leslie; Agarwal, Aishwarya; Chandran, Aswathy; Chaves, Susana R.; Winkelmann, Juliane; Trenkwalder, Claudia; Schwager, Maike; Pauli, Silke; Dettmer, Ulf; Fernández, Claudio O.; Lautenschläger, Janin; Zweckstetter, Markus; Fernandez‐Busnadiego, Ruben; Mollenhauer, Brit ORCID: https://orcid.org/0000-0001-8437-3645 und Outeiro, Tiago Fleming
(2025):
A Novel α‐Synuclein K58N Missense Variant in a Patient with Parkinson's Disease.
In: Movement Disorders
Zenker, Martin; Horn, Denise; Wieczorek, Dagmar; Allanson, Judith; Pauli, Silke; Burgt, Ineke van der; Doerr, Helmuth-Guenther; Gaspar, Harald; Hofbeck, Michael; Gillessen-Kaesbach, Gabriele; Kock, Andreas; Meinecke, Peter; Mundlos, Stefan; Nowka, Anja; Rauch, Anita; Reif, Silke; Schnakenburg, Christian von; Seidel, Heide; Wehner, Lars-Erik; Zweier, Christiane; Bauhuber, Susanne; Matejas, Verena; Kratz, Christian P.; Thomas, Christoph und Kutsche, Kerstin
(2007):
SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome.
In: Journal of Medical Genetics, Bd. 44: S. 651-656
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