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
SINO Syndrome Causative KIDINS220/ARMS Gene Regulates Adipocyte Differentiation.
Zhang K et al.
Frontiers in Cell and Developmental Biology, 2021
33763417 (PubMed )
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