Showing results 1 to 2 of 2
| Title | Author(s) | Issue Date | |
|---|---|---|---|
A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia Journal:Journal of Medical Genetics | 2014 | ||
Fragile X syndrome: genetic and clinical profile in the Hong Kong Chinese population Journal:Hong Kong Medical Journal | 1-Jun-2025 |