LINS1

Publications

Chen et al. Identification of a novel nonsense homozygous mutation of LINS1 gene in two sisters with intellectual disability, schizophrenia, and anxiety. Biomed J. 2021;44(6):748-751. DOI: 10.1016/j.bj.2021.08.003. Epub 2021 Aug 24. PMID: 34450347.

Muthusamy et al. A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability. Front Psychiatry. 2020;11:354. DOI: 10.3389/fpsyt.2020.00354. Epub 2020 May 18. PMID: 32499722.

Najmabadi et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature. 2011;478(7367):57-63. DOI: 10.1038/nature10423. PMID: 21937992.

Neuhofer et al. LINS1-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrum. Neurol Genet. 2020;6(5):e500. DOI: 10.1212/NXG.0000000000000500. PMID: 32802957; PMCID: PMC7413627.

Sheth J et al. Novel LINS1 missense mutation in a family with non-syndromic intellectual disability. Am J Med Genet A. 2017;173(4):1041-1046. DOI: 10.1002/ajmg.a.38089. Epub 2017 Feb 9. PMID: 28181389.