Fol. Biol. 2013, 59, 110-115
https://doi.org/10.14712/fb2013059030110
Mutational Analysis of ACTN4, Encoding α-Actinin 4, in Patients with Focal Segmental Glomerulosclerosis Using HRM Method
Crossref Cited-by Linking
- He Zhechi, Wu Ke, Xie Wenqing, Chen Jianghua: Case report and literature review: A de novo pathogenic missense variant in ACTN4 gene caused rapid progression to end-stage renal disease. Front. Pediatr. 2022, 10. <https://doi.org/10.3389/fped.2022.930258>
- Lin Yu-Hua, Huang Chia-Yen, Ke Chih-Chun, Wang Ya-Yun, Lai Tsung-Hsuan, Liu Hsuan-Che, Ku Wei-Chi, Chan Chying-Chyuan, Lin Ying-Hung: ACTN4 Mediates SEPT14 Mutation-Induced Sperm Head Defects. Biomedicines 2020, 8, 518. <https://doi.org/10.3390/biomedicines8110518>