Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

BACKGROUND: Congenital heart disease (CHD) occurs in almost 1% of newborn children and is considered a multifactorial disorder. CHD may segregate in families due to significant contribution of genetic factors in the disease etiology. The aim of the study was to identify pathophysiological mechanisms...

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Detalles Bibliográficos
Autores principales: Izarzugaza, Jose M. G., Ellesøe, Sabrina G., Doganli, Canan, Ehlers, Natasja Spring, Dalgaard, Marlene D., Audain, Enrique, Dombrowsky, Gregor, Banasik, Karina, Sifrim, Alejandro, Wilsdon, Anna, Thienpont, Bernard, Breckpot, Jeroen, Gewillig, Marc, Brook, J. David, Hitz, Marc-Phillip, Larsen, Lars A., Brunak, Søren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453558/
https://www.ncbi.nlm.nih.gov/pubmed/32859249
http://dx.doi.org/10.1186/s13073-020-00772-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453558/
https://www.ncbi.nlm.nih.gov/pubmed/32859249
http://dx.doi.org/10.1186/s13073-020-00772-z

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