articleNature GeneticsMar 10, 2003BRONZE OA

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

CDCatherine DodéJLJacqueline LevilliersJDJean‐Michel DupontADAnne De PaepeNLNathalie Le Dû

Hôpital Cochin · Institut Cochin · +17 more institutions

PubMed
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Topics & keywords

Topics
Keywords
  • Kallmann syndrome
  • Biology
  • Genetics
  • Mutation
  • Fibroblast growth factor receptor 1
  • Loss function
  • Hypogonadotropic hypogonadism
  • Gene
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