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