Contribution of Congenital Heart Disorders Associated With Copy Number Variants in Mediating Risk for Brain Developmental Disorders: Evidence From 20-Year Retrospective Cohort Study

Rare pathogenic copy number variants (CNVs) are genetic rearrangements that have been associated with an increased risk for congenital heart disorders (CHDs). However, the association of CNVs with atypical brain development, leading to neurodevelopmental disorders (NDDs), in the presence of CHDs rem...

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Detalles Bibliográficos
Autores principales: Dowden, Luke, Tucker, David, Morgan, Sian, Uzun, Orhan, Syed, Yasir Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319541/
https://www.ncbi.nlm.nih.gov/pubmed/34336942
http://dx.doi.org/10.3389/fcvm.2021.655463

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319541/
https://www.ncbi.nlm.nih.gov/pubmed/34336942
http://dx.doi.org/10.3389/fcvm.2021.655463

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