Expanding the genetic and phenotypic relevance of CLCN4 variants in neurodevelopmental condition: 13 new patients.
He H, Li X, Guzman GA, Bungert-Plümke S, Franzen A, Lin X, Zhu H, Peng G, Zhang H, Yu Y, Sun S, Huang Z, Zhai Q, Chen Z, Peng J, Guzman RE.
He H, et al. Among authors: chen z.
J Neurol. 2024 May 17. doi: 10.1007/s00415-024-12383-4. Online ahead of print.
J Neurol. 2024.
PMID: 38758281