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
Autori principali: | Graham, U, Nesbit, M, Hannan, F, Howles, SA, Thakker, R, Hunter, S |
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Natura: | Journal article |
Pubblicazione: |
2013
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