Hypercalcemia in patients with mutations in NR3C2 and SCNN1B-Reference-Cited by-同舟云学术

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Hypercalcemia in patients with mutations in NR3C2 and SCNN1B

Published:2023-11 Issue:10 Volume:161 Page:458-459
ISSN:2387-0206
Container-title:Medicina Clínica (English Edition)
language:en
Short-container-title:Medicina Clínica (English Edition)

Author:

Sainz de los Terreros Errea Amaya,Madariaga Leire,García-Castaño Alejandro

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. A new mutation, R563Q, of the beta subunit of the epithelial sodium channel associated with low-renin, low-aldosterone hypertension;Rayner;J Hypertens,2003

2. Association of pre-eclampsia with the R563Q mutation of the beta-subunit of the epithelial sodium channel;Dhanjal;BJOG,2006

3. Pseudohypoaldosteronisme type I: a rare cause of failure to thrive [Article in French];Derache;Arch Pediatr,2012

4. PMON316 novel mutation causing pseudohypoaldosteronism type 1 and transient hypercalcemia: a patient report;Wu;J Endocr Soc,2022

5. Hypercalcemia in an infant with pseudohypoaldosteronism type 1;Jeng;J Endocr Soc,2021

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