Work

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome

Year: 2001

Type: article

Source: Human Mutation

DOI: 10.1002/humu.1111

Authors: Olga Beltcheva, Paula Martin, Ulla Lenkkeri, Karl Tryggvason

Institutions: Karolinska Institutet, University of Oulu

Language: English

Topic: Renal Diseases and Glomerulopathies

Subfield: Nephrology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Institute of Diabetes and Digestive and Kidney Diseases

Award: NEPHRIN AND KIDNEY FUNCTION AND DISEASE

OpenAlex ID: W2078298967

FWCI: 9.864

Cites: 15

Cited by: 186

Related to: 10