Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM
Beyhan Tüysüz, Adife Gülhan Ercan-Sençicek, Emre Özer, Nükte Göç, Cengiz Yalçınkaya, Kaya Bilguvar
(Turk Arch Pediatr 2022; 57: 521-525) DOI: 10.5152/TurkArchPediatr.2022.22070