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 WangPublished 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.