Characterising heart rhythm abnormalities associated with Xp22.31 deletion

BACKGROUND: Genetic deletions at Xp22.31 are associated with the skin condition X linked ichthyosis (XLI), and with a substantially increased risk of atrial fibrillation/flutter (AF), in males. AF is associated with elevated thrombosis, heart failure, stroke and dementia risk. METHODS: Through: (a)...

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Detalles Bibliográficos
Autores principales: Wren, Georgina, Baker, Emily, Underwood, Jack, Humby, Trevor, Thompson, Andrew, Kirov, George, Escott-Price, Valentina, Davies, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Genotype-Phenotype Correlations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359567/
https://www.ncbi.nlm.nih.gov/pubmed/36379544
http://dx.doi.org/10.1136/jmg-2022-108862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359567/
https://www.ncbi.nlm.nih.gov/pubmed/36379544
http://dx.doi.org/10.1136/jmg-2022-108862

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