Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative effects-Reference-Cited by-同舟云学术

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

Published:2015-06-16 Issue:18 Volume:24 Page:5079-5092
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Hannan Fadil M.,Howles Sarah A.,Rogers Angela,Cranston Treena,Gorvin Caroline M.,Babinsky Valerie N.,Reed Anita A.,Thakker Clare E.,Bockenhauer Detlef,Brown Rosalind S.,Connell John M.,Cook Jacqueline,Darzy Ken,Ehtisham Sarah,Graham Una,Hulse Tony,Hunter Steven J.,Izatt Louise,Kumar Dhavendra,McKenna Malachi J.,McKnight John A.,Morrison Patrick J.,Mughal M. Zulf,O'Halloran Domhnall,Pearce Simon H.,Porteous Mary E.,Rahman Mushtaqur,Richardson Tristan,Robinson Robert,Scheers Isabelle,Siddique Haroon,van't Hoff William G.,Wang Timothy,Whyte Michael P.,Nesbit M. Andrew,Thakker Rajesh V.

Funder

United Kingdom Medical Research Council (MRC)

National Institute for Health Research

NIHR

Wellcome Trust Clinical Training Fellows

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/18/5079/2007260/ddv226.pdf

Reference34 articles.