Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism
Ute I. Scholl(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Richard P. Lifton(Rockefeller University), Peyman Björklund(Uppsala University), Erin Loring(Howard Hughes Medical Institute), Gerald Goh(Yale University), Christoph Fahlke(Forschungszentrum Jülich), Gunnar Westin(Uppsala University Hospital), Lee F. Starker(Uppsala University), Reju Korah(Yale University), John D. Overton(Yale University), Annabelle L. Fonseca(Yale Cancer Center), Tobias Carling(West Health), Carol Nelson‐Williams(Howard Hughes Medical Institute), Patricia Hidalgo(Forschungszentrum Jülich), Nelly Mauras(Nemours Children's Clinic), Shrikant Mane(Yale Cancer Center), Per Hellman(Uppsala University Hospital), Erum A. Hartung(Children's Hospital of Philadelphia), Manju L. Prasad(Yale University), Matthew Benson(Nemours Children's Clinic), Göran Åkerström(Uppsala University), Gabriel Stölting(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), John W. Kunstman(University of New Haven), Regina Campos de Oliveira(Medizinische Hochschule Hannover), Jay R. Shapiro(The University of Texas at Austin), Murim Choi(Seoul National University), Tammy M. Brady(Johns Hopkins University), Steven K. Libutti(Unknown)
Cited by 621
Related Papers
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
|Neuron|2015|1.5k
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
|Neuron|2011|1.3k
Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
|Cell|1994|1.3k
Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting
|European Journal of Endocrinology|2017|1.1k