Work

Dent Disease with Mutations in OCRL1

Year: 2005

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/427887

Authors: Richard R. Hoopes, Antony E. Shrimpton, Stephen J. Knohl, Paul Hueber, Bernd Hoppe, Janos Matyus, Ari Simckes, Velibor Tasic, Burkhard Toenshoff, Sharon F. Suchy, Robert L. Nussbaum, Steven J. Scheinman

Institutions: SUNY Upstate Medical University, University of Cologne, University of Debrecen, Children's Mercy Hospital, Ss. Cyril and Methodius University in Skopje, University Hospital Heidelberg, National Institutes of Health, National Human Genome Research Institute

Language: English

Topic: Ion Transport and Channel Regulation

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funder: National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G1862962940, CLC-5 Inactivation and Hypercalciuria in Dent's Disease

OpenAlex ID: W2166610047

FWCI: 6.15

Cites: 28

Cited by: 335

Related to: 10