1. Chen, Yu-Jie, Wang, Wen-Jie, Zou, Dong-Fang, Li, Bin, Chen, Yong-Jun. 2024. CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. In Clinical genetics, 105, 397-405. doi:10.1111/cge.14476. https://pubmed.ncbi.nlm.nih.gov/38173219/
2. Caputo, Donatella, Cetica, Valentina, Paoli, Silvia, Rosati, Anna, Lazzeri, Simone. 2023. Confirmation of the Pathogenetic Role of the CCDC88C Gene in Early-Onset Pure Spastic Paraplegia. In Movement disorders : official journal of the Movement Disorder Society, 38, 1561-1562. doi:10.1002/mds.29459. https://pubmed.ncbi.nlm.nih.gov/37317935/
3. Yahia, Ashraf, Chen, Zhefan Stephen, Ahmed, Ammar E, Chan, Ho Yin Edwin, Stevanin, Giovanni. 2021. A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report. In BMC neurology, 21, 78. doi:10.1186/s12883-021-02113-y. https://pubmed.ncbi.nlm.nih.gov/33602173/
4. Leńska-Mieciek, Marta, Charzewska, Agnieszka, Królicki, Leszek, Gambin, Tomasz, Fiszer, Urszula. 2018. Familial ataxia, tremor, and dementia in a polish family with a novel mutation in the CCDC88C gene. In Movement disorders : official journal of the Movement Disorder Society, 34, 142-144. doi:10.1002/mds.27536. https://pubmed.ncbi.nlm.nih.gov/30398676/
5. Deng, Boya, Zhang, Siyang, Zhou, Yingying, Li, Ailin, Miao, Yuan. 2024. CCDC88C, an O-GalNAc glycosylation substrate of GALNT6, drives breast cancer metastasis by promoting c-JUN-mediated CEMIP transcription. In Cancer cell international, 24, 237. doi:10.1186/s12935-024-03413-2. https://pubmed.ncbi.nlm.nih.gov/38971758/
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