Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/106709
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Gagliardi, L. | - |
dc.contributor.author | Burt, M. | - |
dc.contributor.author | Feng, J. | - |
dc.contributor.author | Poplawski, N. | - |
dc.contributor.author | Scott, H. | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Clinical Endocrinology, 2016; 85(3):495-497 | - |
dc.identifier.issn | 0300-0664 | - |
dc.identifier.issn | 1365-2265 | - |
dc.identifier.uri | http://hdl.handle.net/2440/106709 | - |
dc.description | Letter to the Editor | - |
dc.description.statementofresponsibility | Lucia Gagliardi, Morton G. Burt, Jinghua Feng, Nicola K. Poplawski and Hamish S. Scott | - |
dc.language.iso | en | - |
dc.publisher | Wiley-Blackwell | - |
dc.rights | © 2016 John Wiley & Sons Ltd | - |
dc.source.uri | http://dx.doi.org/10.1111/cen.13104 | - |
dc.subject | Humans | - |
dc.subject | Hypocalcemia | - |
dc.subject | Receptors, Calcium-Sensing | - |
dc.subject | Pedigree | - |
dc.subject | Mutation | - |
dc.subject | Middle Aged | - |
dc.subject | Female | - |
dc.subject | Fractures, Bone | - |
dc.title | Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1111/cen.13104 | - |
dc.relation.grant | http://purl.org/au-research/grants/nhmrc/1023059 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Poplawski, N. [0000-0002-9372-3325] | - |
dc.identifier.orcid | Scott, H. [0000-0002-5813-631X] | - |
Appears in Collections: | Aurora harvest 3 Medicine publications |
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