Mental retardation and microcephaly with pontine and cerebellar hypoplasia - Wikipedia
Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH) | PLOS ONE
Kicking CASK - Rare Disease Day 2023
CASK Gene - GeneCards | CSKP Protein | CSKP Antibody
Sophia's Story: MAGEC Growing Rod Implantation to Treat Neuromuscular Scoliosis | Children's Hospital of Philadelphia
CASK-related intellectual disability: MedlinePlus Genetics
Faces of CASK — CASK Gene Foundation
Girl with Cask gene mutation affecting only FIVE kids in UK unlikely to ever walk or talk | UK | News | Express.co.uk
CASK Gene Mutation | Latest Research & Resources
Cells | Free Full-Text | The Non-Linear Path from Gene Dysfunction to Genetic Disease: Lessons from the MICPCH Mouse Model
Brave teenage girl, 13, dies on the Disney holiday of her dreams | Daily Mail Online
Phenotypic spectrum associated with CASK loss-of-function mutations | Journal of Medical Genetics
CASK Functions as a Mg2+-Independent Neurexin Kinase: Cell
CASK - Wikipedia
Cask gene mutation | Cask mutation | Beacon for rare diseases
Regulation of Liprin-α phase separation by CASK is disrupted by a mutation in its CaM kinase domain | Life Science Alliance
Phenotypic and molecular insights into CASK-related disorders in males | Request PDF
Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient | Orphanet Journal of Rare Diseases | Full Text
Girl with Cask gene mutation affecting only FIVE kids in UK unlikely to ever walk or talk | UK | News | Express.co.uk
Girl with Cask gene mutation affecting only FIVE kids in UK unlikely to ever walk or talk | UK | News | Express.co.uk
Enora's Story: CASK-related disorders - EURORDIS
Virginia Tech clinic gives hope to children struggling with rare diseases
CASK-related intellectual disability: MedlinePlus Genetics
