Contribution of LRP1 in Human Congenital Heart Disease Correlates with Its Roles in the Outflow Tract and Atrioventricular Cushion Development

Due to the prevalence of congenital heart disease in the human population, determining the role of variants in congenital heart disease (CHD) can give a better understanding of the cause of the disorder. A homozygous missense mutation in the LDL receptor-related protein 1 (Lrp1) in mice was shown to...

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Detalles Bibliográficos
Autores principales: Arrigo, Angelo B., Zhu, Wenjuan, Williams, Kylia A., Guzman-Moreno, Carla, Lo, Cecilia, Lin, Jiuann-Huey I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137934/
https://www.ncbi.nlm.nih.gov/pubmed/37107705
http://dx.doi.org/10.3390/genes14040947

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137934/
https://www.ncbi.nlm.nih.gov/pubmed/37107705
http://dx.doi.org/10.3390/genes14040947

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