Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
Work
Year: 2003
Type: article
Source: Nature Genetics
Authors Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont, Anne De Paepe, Nathalie Le Dû +25 more
Institutions Institut Cochin, Hôpital Cochin, Centre de Référence Déficits Immunitaires Héréditaires, Institut Pasteur, Ghent University Hospital +14 more
Cites: 15
Cited by: 817
Related to: 10
FWCI: 15.89
Citation percentile (by year/subfield): 100
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze