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Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene

Publication status:
Published

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Institution:
University of Oxford
Department:
Oxford, MSD, RDM, OCDEM
Role:
Author
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Journal:
IRISH JOURNAL OF MEDICAL SCIENCE
Volume:
182
Pages:
S421-S421
Publication date:
2013-11-05
ISSN:
0021-1265
URN:
uuid:6f956c0e-7e4f-40e7-a641-aab3b10dc465
Source identifiers:
436841
Local pid:
pubs:436841

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