Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia Journal:Journal of Medical Genetics | 2014 | ||
2021 | |||
2023 |
Title | Author(s) | Issue Date | |
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A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia Journal:Journal of Medical Genetics | 2014 | ||
2021 | |||
2023 |