Associated Papers
Identification of a Novel Missense Homozygous Variant in LINS1 in Two Distinct Iranian Families With Consanguineous Marriage.
Alimoradi E et al.
Molecular Genetics & Genomic Medicine, 2026
Domain-specific phenotypes in LINS1-related disorder-A Chinese family with the Q92X variant and literature review.
Li XY et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2024
Identification of a novel nonsense homozygous mutation of LINS1 gene in two sisters with intellectual disability, schizophrenia, and anxiety.
Chen CH et al.
Biomedical Journal, 2021
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