Work

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ–5)

Year: 1994

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng0394-299

Authors: Daniel Aberdam, Marie-Florence Galliano, Joëlle Vailly, Leena Pulkkinen, Jeannette Bonifas, Angela M. Christiano, Karl Tryggvason, Jouni Uitto, Ervin H. Epstein, Jean-Paul Ortonne, Guerrino Meneguzzi

Institutions: Inserm, Thomas Jefferson University, Kuopio University Hospital, San Francisco General Hospital, University of California, San Francisco, University of Oulu

Language: English

Topic: Skin and Cellular Biology Research

Subfield: Cell Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases

Awards: EPIDERMOLYSIS BULLOSA SIMPLEX--GENETIC ANALYSIS, G1991966960, Program Project Grant, G6585885163

OpenAlex ID: W2072041699

FWCI: 15.92

Cites: 37

Cited by: 334

Related to: 10