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Autor:
Roger A Barker, Laura Oakley, Emma Cutting, David C Rubinsztein, Dimitrios Apostolopoulos, Nikolaos Demiris, Katie Andresen, Amy H Evans, Alimu Dayimu, Katherine Bongaerts, Robyn Staples, Wendy Gooding
Publikováno v:
BMJ Open, Vol 14, Iss 8 (2024)
Introduction Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder that presents with a progressive movement disorder along with cognitive and psychiatric problems. It is caused by a Cytosine-adenin-guanine (CAG) expansion i
Externí odkaz:
https://doaj.org/article/589e70e6f6874d20a47a4fc3a9577f30