A Family with Autosomal Dominant Hypocalcaemia with Hypercalciuria (ADHH): Mutational Analysis, Phenotypic Variability and Treatment Challenges
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.2005.18.7.689/pdf
Reference34 articles.
1. Idiopathic Hypoparathyroidism with Cataract and Spontaneous Hypocalcaemic Hypercalciuria
2. Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation
3. Calcium-sensing receptor in the rat hippocampus: a developmental study
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