Work

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

Year: 2011

Type: article

Study design: Observational Study

Source: Kidney International

DOI: 10.1038/ki.2011.297

Authors: Rasheed A. Gbadegesin, Peter J. Lavin, Gentzon Hall, Bartlomiej Bartkowiak, Alison Homstad, Ruiji Jiang, Guanghong Wu, Alison Byrd, Kelvin Lynn, Norman Wolfish, Carolina Ottati, Paul Stevens, David Howell, Peter Conlon, Michelle P. Winn

Institutions: Duke Medical Center, Christchurch Hospital, Children's Hospital of Eastern Ontario, Beaumont Hospital

Language: English

Topic: Renal Diseases and Glomerulopathies

Subfield: Nephrology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Nephcure Foundation, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: A New Locus for Hereditary FSGS on Chromosome 2p, Center for Molecular & Cellular Studies of Ped Disease

OpenAlex ID: W2012997980

FWCI: 5.365

Cites: 21

Cited by: 76

Related to: 10