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Cdc42GAP deficiency contributes to the Alzheimer's disease phenotype.
Zhu M, Xiao B, Xue T, Qin S, Ding J, Wu Y, Tang Q, Huang M, Zhao N, Ye Y, Zhang Y, Zhang B, Li J, Guo F, Jiang Y, Zhang L, Zhang L. Zhu M, et al. Among authors: li j. Brain. 2023 Oct 3;146(10):4350-4365. doi: 10.1093/brain/awad184. Brain. 2023. PMID: 37254741
Investigation of FRMPD4 variants associated with X-linked epilepsy.
Li RK, Li H, Tian MQ, Li Y, Luo S, Liang XY, Liu WH, Li BM, Shi XQ, Li J, Li B, Shu XM; China Epilepsy Gene 1.0 Project. Li RK, et al. Among authors: li y, li j, li h, li bm, li b. Seizure. 2024 Mar;116:45-50. doi: 10.1016/j.seizure.2023.05.014. Epub 2023 Jun 10. Seizure. 2024. PMID: 37330374
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