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Article

Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications.

Clinical endocrinology - 1 Sept 2016

Gagliardi Lucia, Burt Morton G, Feng Jinghua, Poplawski Nicola K, Scott Hamish S

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Share to Fractures, Bone
Share to CASR gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Receptors, Calcium-Sensing

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Identifiers

PMID: 27177819
DOI: 10.1111/cen.13104

Genes

CASR

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Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications.PMID 27177819Read ↗

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Autosomal dominant hypocalcemia with a novel CASR mutation: a case study and literature review.Semantic proximity Read ↗

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A Novel Activating Mutation in Calcium-Sensing Receptor Gene Associated with a Family of Autosomal Dominant Hypocalcemia1Semantic proximity Read ↗

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CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.Semantic proximity Read ↗

A novel mutation of the calcium-sensing receptor gene in a Greek family from Nisyros.Semantic proximity Read ↗

A novel homozygous inactivating mutation of the calcium-sensing receptor causing familial hypocalciuric hypercalcemia complicated with primary hyperparathyroidism due to parathyroid adenoma: A case report.Semantic proximity Read ↗

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