Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series.
- Resource Type
- Article
- Source
- Neurogenetics; Apr2022, Vol. 23 Issue 2, p115-127, 13p
- Subject
AMELOGENESIS imperfecta PYRAMIDAL tract CORPUS callosum SPASTICITY MOVEMENT disorders MEDICAL records GENETIC mutation - Language
- ISSN
- 13646745