Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Nicole Martin-Kenny"'
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-14 (2023)
Abstract Background ATRX is an ATP-dependent chromatin remodeling protein with essential roles in safeguarding genome integrity and modulating gene expression. Deficiencies in this protein cause ATR-X syndrome, a condition characterized by intellectu
Externí odkaz:
https://doaj.org/article/c55c566f07c34869b908fefa16aa23e7
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-11 (2020)
Abstract Background Alpha-thalassemia/mental retardation, X-linked, or ATRX, is an autism susceptibility gene that encodes a chromatin remodeler. Mutations of ATRX result in the ATR-X intellectual disability syndrome and have been identified in autis
Externí odkaz:
https://doaj.org/article/bcb2c66f020b4ae1ac947fb682503047
Publikováno v:
Paediatrics Publications
α-Thalassemia X-linked intellectual disability (ATR-X) syndrome is a neurodevelopmental disorder caused by mutations in the ATRX gene that encodes a SNF2-type chromatin-remodeling protein. The ATRX protein regulates chromatin structure and gene expr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d782febc23f02d631de5e7e01d82ab1c
https://ir.lib.uwo.ca/paedpub/489
https://ir.lib.uwo.ca/paedpub/489
