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Oxford University Press (OUP), Human Molecular Genetics, 18(24), p. 5079-5092

DOI: 10.1093/hmg/ddv226

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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

Journal article published in 2015 by Fadil M. Hannan, Sarah A. Howles, Angela Rogers, Treena Cranston, Caroline M. Gorvin, Valerie N. Babinsky, Anita A. Reed, Clare E. Thakker, Detlef Bockenhauer, Rosalind S. Brown, John M. Connell, Jacqueline Cook, Ken Darzy, Sarah Ehtisham, Una Graham and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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