Moonwalker Mouse
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-15070-8_69
Reference42 articles.
1. Becker EBE (2020) Moonwalker mouse. In: Manto M, Gruol D, Schmahmann J, Koibuchi N, Sillitoe R (eds) Handbook of the cerebellum and cerebellar disorders. Springer, Cham. https://doi.org/10.1007/978-3-319-97911-3_107-1
2. Becker EBE, Oliver PL, Glitsch MD, Banks GT, Achilli F, Hardy A, Nolan PM, Fisher EMC, Davies KE (2009) A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proc National Acad Sci U S A 106(16):6706–6711
3. Bird TD (2015) Hereditary ataxia overview. In: Adam MP, Ardinger HH, Pagon RA et al (eds) GeneReviews®. University of Washington, Seattle, WA, pp 1993–2021
4. Brooker SM, Edamakanti CR, Akasha SM, Kuo S-H, Opal P (2021) Spinocerebellar ataxia clinical trials: opportunities and challenges. Ann Clin Transl Neur 8(7):1543–1556
5. Cederholm JME, Kim Y, von Jonquieres G, Housley GD (2019) Human brain region-specific alternative splicing of TRPC3, the type 3 canonical transient receptor potential non-selective cation channel. Cerebellum 18(3):536–543
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