1. Li, Weiquan, Meng, Xiangui, Yuan, Hongwei, Xiao, Wen, Zhang, Xiaoping. 2022. M2-polarization-related CNTNAP1 gene might be a novel immunotherapeutic target and biomarker for clear cell renal cell carcinoma. In IUBMB life, 74, 391-407. doi:10.1002/iub.2596. https://pubmed.ncbi.nlm.nih.gov/35023290/
2. Laquerriere, Annie, Jaber, Dana, Abiusi, Emanuela, Gitiaux, Cyril, Melki, Judith. 2021. Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita. In Journal of medical genetics, 59, 559-567. doi:10.1136/jmedgenet-2020-107595. https://pubmed.ncbi.nlm.nih.gov/33820833/
3. Zhang, Ying, Yang, Shuya, Huo, Xiaodong, Liao, Shixiu, Hou, Qiaofang. . [Analysis of CNTNAP1 gene variants in a Chinese pedigree affected with lethal congenital contracture syndrome type 7]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 39, 194-197. doi:10.3760/cma.j.cn511374-20201021-00739. https://pubmed.ncbi.nlm.nih.gov/35076918/
4. Wang, Helen, Chen, Dillon, Del Campo, Miguel, Del Rosario, Pamela, Lee, Pei-Shan. 2024. Novel CNTNAP1 gene variant identified in congenital hypomyelinating neuropathy-3: A case report. In SAGE open medical case reports, 12, 2050313X241302236. doi:10.1177/2050313X241302236. https://pubmed.ncbi.nlm.nih.gov/39583069/
5. Hengel, Holger, Magee, Alex, Mahanjah, Muhammad, Sharkia, Rajech, Schöls, Ludger. 2017. CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis. In Neurology. Genetics, 3, e144. doi:10.1212/NXG.0000000000000144. https://pubmed.ncbi.nlm.nih.gov/28374019/
6. Letko, Anna, Minor, Katie M, Friedenberg, Steven G, Mickelson, James R, Drögemüller, Cord. 2020. A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy. In Genes, 11, . doi:10.3390/genes11121426. https://pubmed.ncbi.nlm.nih.gov/33261176/
智鼠故事 
