Submit a Response to This Article
Jump to comment:
No eLetters have been published for this article.
In this issue
Jump to section
Related Articles
Cited By...
- Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein
- Complete loss of the X-linked gene CASK causes severe cerebellar degeneration
- Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study
- Complete loss of CASK causes severe ataxia through cerebellar degeneration in human and mouse
- Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution
- Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI
- Phenotypic spectrum associated with CASK loss-of-function mutations