Involvement of casein kinase 1 epsilon/delta (Csnk1e/d) in the pathogenesis of familial Parkinson's disease caused by CHCHD2
Abstract Parkinson's disease (PD) is a common neurodegenerative disorder that results from the loss of dopaminergic neurons. Mutations in coiled‐coil‐helix‐coiled‐coil‐helix domain containing 2 (CHCHD2) gene cause a familial form of PD with α‐Synuclein aggregation, and we here identified the pa...
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          | Main Authors: | , , , , , , , , , , , | 
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| Format: | Article | 
| Language: | English | 
| Published: | Springer Nature
    
        2023-08-01 | 
| Series: | EMBO Molecular Medicine | 
| Subjects: | |
| Online Access: | https://doi.org/10.15252/emmm.202317451 | 
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