DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder
Author:
Funder
Ontario Genomics Institute
Ministero dell’Istruzione, dell’Università e della Ricerca
Genome Canada
Government of Canada
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference46 articles.
1. Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability;Bramswig;Hum Genet,2017
2. Expanding the phenotype of HNRNPU-related neurodevelopmental disorder with emphasis on seizure phenotype and review of literature;Taylor;Am J Med Genet A,2022
3. Molecular basis for the specific and multivariant recognitions of RNA substrates by human hnRNP A2/B1;Wu;Nat Commun,2018
4. HnRNP Q Has a suppressive role in the translation of mouse Cryptochrome1;Lim;PLoS One,2016
5. The hnRNP family: insights into their role in health and disease;Geuens;Hum Genet,2016
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