Associated Papers
Detection of pathogenic novel intronic splicing variants in the KIDINS220 gene causes motor developmental delay.
Bai L et al.
Artificial Cells, Nanomedicine, and Biotechnology, 2026
Pure Hereditary Spastic Paraplegia in a Patient With a Novel Heterozygous KIDINS220 Gene Mutation.
Al Hussein HS et al.
Cureus, 2024
Prefrontal neuronal integrity predicts symptoms and cognition in schizophrenia and is sensitive to genetic heterogeneity.
Malaspina D et al.
Schizophrenia Research, 2016
Rare variants in the neurotrophin signaling pathway implicated in schizophrenia risk.
Kranz TM et al.
Schizophrenia Research, 2015
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