Absence of pathogenic calcium sensing receptor mutations in sporadic idiopathic hypoparathyroidism
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2006.02604.x/fullpdf
Reference23 articles.
1. Hypoparathyroidism in the Differential Diagnosis of Hypocalcemia
2. A deletion in chromosome 22 can cause digeorge syndrome
3. APS-I/APECED: the clinical disease and therapy
4. Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
5. Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation
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2. Vertebral fractures and bone mineral density in patients with idiopathic hypoparathyroidism on long term follow-up;The Journal of Clinical Endocrinology & Metabolism;2016-11-04
3. Presence of Auto-reactive, MHC class-I restricted, Calcium Sensing Receptor (CaSR) specific CD8+ T cells in Idiopathic Hypoparathyroidism;The Journal of Clinical Endocrinology & Metabolism;2016-11-02
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5. Calcium-sensing receptor sequencing in 21 patients with idiopathic or familial parathyroid disorder: pitfalls and characterization of a novel I32 V loss-of-function mutation;Endocrine;2014-08-05
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