Identification and structural characterisation of a novel mutation in the CNKSR2 gene associated with Houge-Type X-Linked Intellectual Developmental Disorder
Fields of Study & Subjects
Genomics and Rare Diseases
Genetics and Neurodevelopmental Disorders
Genomic variations and chromosomal abnormalities
Publication details
- Journal / source
- Journal of Human Genetics
- Publisher
- Springer Science and Business Media LLC
- Volume
- 71
- Issue
- 8
- Pages
- 501–512
- Publication date
- 7 April 2026
- Language
- EN