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

Concepedia

Publication | Open Access

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

DOI Full Paper Access

825

Citations

12

References

2003

Year

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont, Anne De Paepe, Nathalie Le Dû, Nadia Soussi‐Yanicostas, Roney S. Coimbra, Sedigheh Delmaghani, Sylvie Compain-Nouaille, Françoise Baverel,

Nature Genetics

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsLoss-of-function MutationsMedicine

References

	Year	Citations

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