Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E. Schaffer, Joseph G. Gleeson, Cahide Yılmaz et al.|Nature Genetics|2018Cited by 87
Evaluation of Pediatric Cases With Gullian Barre Syndrome: A National Multicenter Study.Çisil Çerçi Kubur, LEMAN TEKİN ORGUN, Fatma Hanci et al.|Kocaeli Üniversitesi - AVESİS|2022Cited by 0
Evaluation Of Pediatric Cases With Gullian Barre Syndrome: A National Multicenter StudyMuhittin Bodur, Mehmet Canpolat, . Turkish Pediatric Guillain Barre Study Group Collaboration et al.|Bursa Uludag University - AVESIS|2022Cited by 0