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Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effects. (2015)

First Author: Hannan FM

Attributed to: CIMA: The Centre for Integrated Research into Musculoskeletal Ageing funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddv226

PubMed Identifier: 26082470

Publication URI: http://europepmc.org/abstract/MED/26082470

Type: Journal Article/Review

Volume: 24

Parent Publication: Human molecular genetics

Issue: 18

ISSN: 0964-6906