Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/106709
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Type: Journal article
Title: Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications
Author: Gagliardi, L.
Burt, M.
Feng, J.
Poplawski, N.
Scott, H.
Citation: Clinical Endocrinology, 2016; 85(3):495-497
Publisher: Wiley-Blackwell
Issue Date: 2016
ISSN: 0300-0664
1365-2265
Statement of
Responsibility: 
Lucia Gagliardi, Morton G. Burt, Jinghua Feng, Nicola K. Poplawski and Hamish S. Scott
Keywords: Humans; Hypocalcemia; Receptors, Calcium-Sensing; Pedigree; Mutation; Middle Aged; Female; Fractures, Bone
Description: Letter to the Editor
Rights: © 2016 John Wiley & Sons Ltd
RMID: 0030048263
DOI: 10.1111/cen.13104
Grant ID: http://purl.org/au-research/grants/nhmrc/1023059
Appears in Collections:Medicine publications

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