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pro vyhledávání: '"Jason Hulen"'
Autor:
Jason Hulen, Dorothy Kenny, Rebecca Black, Jodi Hallgren, Kelley G. Hammond, Eric C. Bredahl, Rochelle N. Wickramasekara, Peter W. Abel, Holly A. F. Stessman
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Disruptive variants in lysine methyl transferase 5B (KMT5B/SUV4-20H1) have been identified as likely-pathogenic among humans with neurodevelopmental phenotypes including motor deficits (i.e., hypotonia and motor delay). However, the role that this en
Externí odkaz:
https://doaj.org/article/4323b61daabf460498ad0673e56a7d9f
Publikováno v:
Autism Res
Lysine methyl transferase 5B (KMT5B) has been recently highlighted as a risk gene in genetic studies of neurodevelopmental disorders (NDDs), specifically, autism spectrum disorder (ASD) and intellectual disability (ID); yet, its role in the brain is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb13796833331ea2013b0e90cfa62c08
https://pubmed.ncbi.nlm.nih.gov/33871180
https://pubmed.ncbi.nlm.nih.gov/33871180
Publikováno v:
Journal of Obstetric, Gynecologic & Neonatal Nursing. 47:S58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a0950299fe3a3e6a05970d2cf0522b2
https://doi.org/10.1016/j.jogn.2018.04.114
https://doi.org/10.1016/j.jogn.2018.04.114