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

Document Type

Article

Author

Capri, Y.; Bourmance, L.; Testa, N.; Melki, J.; Kwon, T.; Baudouin, V.; Boyer, O.; Couderc, A.; Heidet, L.; Bonnefoy, R.; Meziane, C.; Tournier-Lasserve, E.

Source

In: Journal of Medical Genetics. (Journal of Medical Genetics, 1 October 2023, 60(10):993-998)

Subject

Language

English

ISSN

14686244
00222593

Online Access

Full Text (BMJ Journals) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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