Associated Papers
Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability.
Khosrowabadi E et al.
Human Molecular Genetics, 2024
Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants.
Khan A et al.
Genes, 2020
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.
Reuter MS et al.
Jama Psychiatry, 2017
NDST1 missense mutations in autosomal recessive intellectual disability.
Reuter MS et al.
American Journal of Medical Genetics. Part A, 2014
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