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pro vyhledávání: '"Moritz Heidenblut"'
Autor:
Felix P. Bernhard, Sven Schütte, Moritz Heidenblut, Moritz Oehme, Susanne Rinné, Niels Decher
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
Potassium channel mutations play an important role in neurological diseases, such as spinocerebellar ataxia (SCA). SCA is a heterogeneous autosomal-dominant neurodegenerative disorder with multiple sub-entities, such as SCA13, which is characterized
Externí odkaz:
https://doaj.org/article/4d8a875cb22245c8b1fb63d635085c5e
