Identification of rare missense variants in the BSN gene co‐segregating with chronic otitis media in a consanguineous Pakistani family
Article in Molecular Genetics & Genomic Medicine (September 2024)
The most recent citing publications are shown below. View all 11 publications that cite this research output on Dimensions.
Behavioral and histological analyses of the mouse Bassoon p.P3882A mutation corresponding to the human BSN p.P3866A mutation
Article in Frontiers in Neuroscience (July 2024)
Reprint of: Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders
Article in Seizure (March 2024)