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Paper Details

Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder.
Genet Med
3
2023
5-methylcytosine, Drosophila, L-methionine, NSUN methyltransferases, NSUN2, NSUN3, NSUN6, NSUN6 ortholog, S-adenosyl-, autosomal recessive intellectual disability, autosomal recessive neurodevelopmental disorder, behavioral anomalies, developmental delay, exon, first, intellectual disability, locomotion and learning impairment, messenger RNAs, methyl, motor delay, neurodevelopmental diseases, neurodevelopmental disorder, transfer RNAs
Author NameAffiliation
Laure Raymond
Stylianos E AntonarakisUniversity of Geneva Medical Faculty, Swiss Institute of Genomic Medicine
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne
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