Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

BACKGROUND: Pathogenic variants of the lysine acetyltransferase 6A or KAT6A gene are associated with a newly identified neurodevelopmental disorder characterized mainly by intellectual disability of variable severity and speech delay, hypotonia, and heart and eye malformations. Although loss of func...

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Detalles Bibliográficos
Autores principales: Urreizti, Roser, Lopez-Martin, Estrella, Martinez-Monseny, Antonio, Pujadas, Montse, Castilla-Vallmanya, Laura, Pérez-Jurado, Luis Alberto, Serrano, Mercedes, Natera-de Benito, Daniel, Martínez-Delgado, Beatriz, Posada-de-la-Paz, Manuel, Alonso, Javier, Marin-Reina, Purificación, O’Callaghan, Mar, Grinberg, Daniel, Bermejo-Sánchez, Eva, Balcells, Susanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011274/
https://www.ncbi.nlm.nih.gov/pubmed/32041641
http://dx.doi.org/10.1186/s13023-020-1317-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011274/
https://www.ncbi.nlm.nih.gov/pubmed/32041641
http://dx.doi.org/10.1186/s13023-020-1317-9

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