Biallelic NPR1 loss of function variants are responsible for neonatal systemic hypertension

BACKGROUND: Early-onset isolated systemic hypertension is a rare condition of unknown genetic origin. Renovascular, renal parenchymal diseases or aortic coarctation are the most common causes of secondary systemic hypertension in younger children and neonates. We investigated the genetic bases of ea...

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Detalles Bibliográficos
Autores principales: Capri, Yline, Kwon, Theresa, Boyer, Olivia, Bourmance, Lucas, Testa, Noe, Baudouin, Véronique, Bonnefoy, Ronan, Couderc, Anne, Meziane, Chakib, Tournier-Lasserve, Elisabeth, Heidet, Laurence, Melki, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Developmental Defects
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579472/
https://www.ncbi.nlm.nih.gov/pubmed/37080586
http://dx.doi.org/10.1136/jmg-2023-109176

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579472/
https://www.ncbi.nlm.nih.gov/pubmed/37080586
http://dx.doi.org/10.1136/jmg-2023-109176

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