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Further delineation of autosomal recessive intellectual disability syndrome caused by homozygous variant of the NSUN2 gene in a chinese pedigree.

Songyang SunLin ChenYuchuan WangJian WangNiu LiXike Wang
Published in: Molecular genetics & genomic medicine (2020)
These are the first findings of a non-consanguineous Chinese pedigree with a homozygous NSUN2 variant. We expanded the phenotypic spectrum associated with NSUN2 variations.
Keyphrases
  • intellectual disability
  • autism spectrum disorder
  • genome wide
  • copy number